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For more information on Pharmaceuticals Consulting ? Call 1-403-770-1994 or email us
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Find quality Pharmaceuticals consultants, regulatory Pharmaceuticals consultants, Pharmaceuticals attorneys, Pharmaceuticals lawyers, Pharmaceuticals expert wintnesses, Pharmaceuticals auditors, Pharmaceuticals scientists for all your Pharmaceuticals consulting, Pharmaceuticals audits and Pharmaceuticals training such as Pharmaceuticals expert witnesses, regulatory submissions, Pharmaceuticals regulatory compliance, Pharmaceuticals advisory meetings, Pharmaceuticals validation, Pharmaceuticals regulatory actions, Pharmaceuticals exporting, Pharmaceuticals importing, Pharmaceuticals certifications, Pharmaceuticals research, Pharmaceuticals scientific reviews, Pharmaceuticals product developments, Pharmaceuticals quality systems, Pharmaceuticals technology transfers, Pharmaceuticals processes, Pharmaceuticals technical writing, Pharmaceuticals legal services, in countries such as the USA, Canada, Mexico, European Union, United Kingdom, Ireland, China, Japan, Australia, etc.

Pharmaceuticals Regulatory Consulting Requests

Global Regulatory.com has received the following incoming Pharmaceuticals Consulting Requests which need to be fulfilled ! These Pharmaceuticals Consulting Requests are received from a variety of sources ranging from start-up companies to large, multinational corporations actively seeking consultants to perform their Pharmaceuticals consulting services. If your company receives requests that it can not fulfill, please refer them to us! If you have questions, please e-mail Global Regulatory or call 403-770-1994 .
Incoming Pharmaceuticals Consulting Requests
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Pharmaceuticals consulting request description
status
12-000082 University needs pharmaceutical regulatory consultant for price of Filing of NDA(new drug application), ANDA(generic new drug application), IND(investigative new drug), AIND(generic investigative new ( read more ).....
12-000080 Pharmaceutical Manufacturer needs Europe Regulatory Consulting Companies for eRFI for Pharmaceutical Regulatory Intelligence Tool for Europe. ( read more ).....
12-000079 We would like a consultant to assist with developing the protocols and validation of our processes and systems as well as review our SOP's for missing requirements. Quality Systems, Validation, Tra ( read more ).....
12-000074 India GLP consultants in Delhi (North Zone) to get GLP certification at the earliest with best service of consultant. ( read more ).....
12-000071 Pharmaceutical Consultant needed for Investigational drug label review to insure that country specific disclosures or information is included on the label. 4+ projects a month with varying country co ( read more ).....
12-000070 GXP experienced Laboratory instrument Qualification Consultant / Contractor needed for the Qualification of Approximately 250 analytical instruments and instrument systems of varying complexity. The p ( read more ).....
12-000065 INDONESIA REGULATORY CONSULTANT NEEDED FOR REGULATORY SUBMISSION AND MA in Indonesia ( read more ).....
12-000053 FDA Consultant needed for FDA GMP vendor audit in India ( read more ).....
12-000052 India only Regulatory consultant needed ISO,CE MARK,UL MARK,PROCESS DEVELOPMENT ( read more )..... Closed
12-000050 Logistics company needs Brazil Regulatory Consultant for import / export advisory services regarding shipping drugs to Brazil from the UK. We would like to speak with someone regarding a consultancy f ( read more ).....
12-000046 Europe Pharmaceutical regulatory consultant needed to advise on innovator for particular product in Europe ( read more )..... Closed
12-000044 Pharmaceutical Manufacturer needs Pharmaceutical Consultant needed for Local license holder service, NDA submission Life cycle maintenance: variatiosn label updates Review of promotional materials ( read more )..... Closed
12-000041 Global medical information and pharmacovigilance consultant needed to advise on expansion of services to Europe, Canada, and Brazil ( read more ).....
12-000038 FDA Consultant needed for US FDA Registered Agent. Company's clients to complete an FDA FEI application as we carry out QC testing on their drug product that they wish to submit to FDA. To do this, w ( read more )..... Closed
12-000036 FDA consultant located in China needed for FDA advisory services ( read more ).....
12-000024 Clinical Trial Regulatory Consultant needed for Turkey MoH audit of site for clinical and bioequivalence studies ( read more )..... Closed
12-000021 Regulatory consultant needed for registration ( read more )..... Closed
12-000020 Mexico Biological Consultants needed for registering a few of biological products at COFEPRIS (same as US FDA) in Mexico. Regulatory filings. Finshied product, injectables. ( read more ).....
12-000017 Regulatory consultant needed to assist pharmaceutical distributor to distribute product in South Africa and Europe. It is manufactured in the United States. Need necessary approvals to sell the produc ( read more )..... Closed
12-000016 Pharmaceutical Regulatory Consultant needed to advise pharma company with new drug for Neuo-Drugs (Diabetic Neuropathic Pain, Post Herpatic Neuralgia, Migraine, Schizophrenia, Depression Disorder)can ( read more )..... Closed
12-000012 In need of an auditor trainer as part of annual refresher training. ( read more ).....
12-000010 US FDA CONSULTANT NEEDED TO ADVISE ON US FDA REQUIREMENTS FOR TO DISTRIBUTE PRODUCTS BY MANUFACTURING IN OUT OF USA. WHAT IS NEW DIETARY INGREDIENTS. FACITLITY INSPECTION REQUIRED OR NOT. ( read more )..... Closed
12-000008 US FDA Consultant needed for FDA ANDA submission services. We are in the feasibility stage and would like to discuss. ( read more )..... Closed
12-000007 US FDA Consultant needed for FDA Audit training and preparation guidance ( read more )..... Closed
12-000006 Regulatory Consultant needed for registration of biosimilars and search for local agent in the required countries ( read more ).....
12-000003 Middle East Regulatory Advisor needed for advising on registering herbal medicinals with Ministry of Health in UAE and Saudi FDA as Herbal Pharmacy. ( read more ).....
11-000123 Regulatory Consultant needed for Saudi Arabia / GCC. ( read more )..... Closed
11-000118 India college laboratory needs FDA GMP / GLP Consultant needed to assist in certifying Laboratory according to GMP/GLP guidelines. Our College is having ,Graduate, Post -graduate (5 specializations), ( read more )..... Closed
11-000117 Regulatory Consultants needed for MAA/BLA Application/approval, Validation & Qualification, Quality systems Sop writing Process development Regulatory Filings Product registration Pharmacovigilen ( read more )..... Closed
11-000116 Korea Pharmaceutical Manufacturer needs FDA Consultant for FDA submission ( read more )..... Closed
11-000115 Regulatory Consultant needed to advise on labeling and whether a product is a herbal, medicine or food supplement ( read more )..... Closed
11-000103 An European based company requires a US based registered agent to submit an orphan dossier already prepared to the FDA on their behalf. ( read more )..... Closed
11-000101 EU Regulatory Consultant needed for compilation of Module 3 part of a registration dossier for EU. Please provide an approximate price for ( read more )..... Closed
11-000100 France Pharmaceutical Manufacturer needs FDA consultant to assist on preparing FDA cGMP France pharmaceutical manufacutirng site for FDA inspection. French manufacturing sites (production of parentera ( read more )..... Closed
11-000099 EU Regulatory Consultant needed for Mock EU Inspection for biologic product. Company is planning marketing authorisation application for biologic product. ( read more )..... Closed
11-000095 Pharmaceutical Manufacturer needs pharma regulatory consultant with sound knowledge and experience in Saudi Arabia ( read more )..... Closed
11-000088 Sterile Pharmaceutical Manufacturer needs UK UK Regulatory Consultant for UK-MHRA certification of Injectable oncology products ( read more )..... Closed
11-000086 Regulatory Pharmaceutical Consultant needed to provide CTD/eCTD training in Egypt ( read more )..... Closed
11-000081 FDA Consultant needed for Gap analysis of cGMP. Currently in Phase II clinical trial. Request proposal to audit production facility and provide recommendations to meet compliance requirements necesa ( read more )..... Closed
11-000080 Pharmaceutical Regulatory COnsultant needed for 1. Pre-market requirement and documentation submission; 2. Post-market requirement and decision tree of vigilance/ adverse event reporting; 3. Reimbur ( read more )..... Closed
11-000078 Australia Regulatory Consultant needed for Australia TGA Advice and guidance for TGA application forms and documents and labelling requirements for a new product. ( read more )..... Closed
11-000076 Pharmaceutical Company needs Mexico Pharmaceutical Consultant for Registration of prescription pharmaceutical products within Mexico and facilitate direct contact with regulatory authorities ( read more )..... Closed
11-000075 Pharmaceutical company needs Singapore HSA knowledgeable consultant to gain approval from the Singapore HSA for our therapy to reverse chronic stroke damage based primarily upon the results of our pha ( read more )..... Closed
11-000072 Regulatory consultant needed for filing Application for Orphan Drug Designation of a product in Japan. ( read more )..... Closed
11-000066 REGULATORY CONSULTANT NEEDED TO UPGRADE DOSSIER TO EU CTD LEVEL ( read more )..... Closed
11-000065 Pharmaceutical consultant needed for Clinical trial, compassionate use/early access program, regulatory filings, importing of investigational drugs ( read more )..... Closed
11-000058 Pharmaceutical formulation expert with experience in oral liquid formulations and stability needed ( read more )..... Closed
11-000057 Pharmaceutical company planning on launching several products for Japan and S. Korea and EU. Need pharmaceutical consultant to verify the capability of the ingredients to be used in countries. ( read more )..... Closed
11-000055 India Pharmaceutical Mfg needs WHO consultant for WHO compliance ( read more )..... Closed
11-000053 FDA Regulatory Consultant needed for preparing FDA Investigational New Drug Applications, IND submissions for US-FDA. 1) Preparation of IND submission Dossier. 2) Gap analysis and review the prepared ( read more )..... Closed
11-000050 Consultant needed for Clinical labeling of investigational drug ( read more )..... Closed
11-000048 India based regulatory consultant needed for tradition medicinal product registration ( read more )..... Closed
11-000047 SAUDI ARABIA HERBAL COMPANY NEEDS ARCHITECT TO ASSIST IN ESTABLISHING HERBAL MEDICINE PRODUCTS FACTORY IN USA IN ORDER TO MANUFACTRE FOR USA AND SAUDI ARABIA ( read more )..... Closed
11-000045 Asia Regulatory consultant needed to advice large pharma on Fixed Dose Combination registration in Korea with KFDA. Also the services could be expanded to submission and follow up of the application w ( read more )..... Closed
11-000043 Middle East Based Consultant needed for registering products in countries like saudi arabia, united arab emirates, kuwait, etc and also adhering to the requirements of the FDA in each respective count ( read more )..... Closed
11-000042 South America Regulatory Consultant needed for Regulatory Filings in Argentina, Brazil, Mexico, Venezuela and Panama ( read more )..... Closed
11-000041 Pharmaceutical Consultant needed to advise on GCC CDR ( read more )..... Closed
11-000029 TGA consultant needed for Australian TGA Certification - GMP for Medicinal Products ( read more )..... Closed
11-00026 India Pharmaceutical Mfg needs FDA Regulatory Consultant for IND submission and EU CTD, SOP writing ( read more )..... Closed
11-00024 Middle East Pharmaceutical Consultant needed for pharmaceutical registration at MOH UAE ( read more )..... Closed
11-00023 San Diego Biotechnology company needs a virology expert who also has quality assurance background to conduct an audit of a medical laboratory that is in the Netherlands. Would Global Regulatory be ( read more )..... Closed
11-00022 Large Pharma needs India Consultant for OTC and Rx NDA, Manufacturing Licenses, Traditional Medicines Registrations, Food registrations in both Indonesia and India. ( read more )..... Closed
11-00018 Training for regulations and regulatory agencies (e.g., FDA, Homeland Security, Customs, etc.) involved in the importation of medications by manufacturers to help better understand this complex landsc ( read more )..... Closed
11-00016 REGULATORY CONSULTANT NEEDED FOR CTD DOSSIERS SUBMISSIONS TO DCA & LIASION FOR PRODUCT REGISTRATION ( read more )..... Closed
11-00014 Italy Pharmaceutical Manufacturer needs South Korea Pharmaceutical Consultant for pharmaceutical registration in South Korea ( read more )..... Closed
11-00009 Oncology company needs Registered agent/Regulatory Consultant for EMEA or FDA GMP certification of products ( read more )..... Closed
11-00007 Europe Pharmaceutical Consultant needed for Generation of CTA and regulatory advice for small molecule drug (NCE) in the area of Alzheimer's disease to enter clinical phase I in Europe in second half ( read more )..... Closed
11-00003 Freelance Labeling Expert needed to review, create and update all our product information for diverse drugs ( read more )..... Closed
11-00001 Large Consumer Products Mfg needs Regulatory Pharmaceutical Consultant with Expertise to guide development of a regulatory strategy resulting in an FDA NDA submission/aproval for topical antimicrobial ( read more )..... Closed
10-00173 Validation Consultant needed to advise on requirements for qualification of Deionized DI Water System ( read more )..... Closed
10-00169 Regulatory Consultant needed to get CRO-Facility accreditation by MoH,Turkey ( read more )..... Closed
10-00168 Canada Pharmaceutical Consultant needed for Provincial formulary submissions for 5 solid oral dose products ( read more )..... Closed
10-00158 Consultant needed that specializes in Drug Market Authorisation in Europe and Switzerland. I am preparing a business plan for a start up. Thank you for your reply. ( read more )..... Closed
10-00150 India and China Regulatory Consultant needed toevaluate and identify requirements for the dossier assembly and submission of license applications for an existing US OTC to be marketed in India and Chi ( read more )..... Closed
10-00138 Korea Pharmaceutical Mfg needs consulting for the conceptual design of animal laboratory facility that meets GMP-regulation, approved by US FDA and EU. This lab is for quality control test of biopha ( read more )..... Closed
10-00127 India Company needs India Regulatory Consultant to assist in US FDA and NIOSH approval ( read more )..... Closed
10-00124 Health Canada Regulatory Consultant needed ASAP to conduct OTC drug GMP audit to Canadian Drug GMPs is required for an over the counter drug product manufacturer in India. This audit needs to be cond ( read more )..... Closed
10-00123 Attorney or regulatory consulting firm needed for guidance on regulatory, trade mark, patent, pricing for orphan and specialty pharmaceuticals to make a go or no go decision to go into these markets. ( read more )..... Closed
10-00122 Regulatory Consultant needed for otc drug registration requirements for india, u.s, canada, japan. ( read more )..... Closed
10-00121 Regulatory Company needed for FDA ANDA Submission, EU CTD, FDA GMP Vendor Audit, ISO Compliance, Validation & Qualification, Import/Export, Labeling and Advertising Reviews, Quality Systems, SOP Writi ( read more )..... Closed
10-00120 Regulatory Company needed for EC, AEMPS submissions for approval of clinical study approximately 3 sites in Spain ( read more )..... Closed
10-00117 CRO needs regulatory consultant for Anvisa approval of facility. ( read more )..... Closed
10-00114 We are seeking regulatory consultancy services for preparation of OTC herbal drug monograph for a herbal cough syrup.We want your guidance for the technical requirements for compilation of OTC drug mo ( read more )..... Closed
10-00113 Pharmaceutical Manufacturer needs regulatory consultant to advise on registration of pharmaceuticals in Hong Kong ( read more )..... Closed
10-00104 Regulatory Consultant needed to assist in registering Ethical and OTC drug in Australia. ( read more )..... Closed
10-000102 Thailand Pharma Company needs regulatory consultant for HIV drug registration ( read more )..... Closed
10-00097 Homeopathic Combination Manufacturer needs FDA consultant to register these combinations with FDA under OTC Homeopathic Drugs. We need services of assistant to register these combinations according to ( read more )..... Closed
10-00094 Israel company needs regulatory consultant for Regulatory compliance and Filings for import of Hand Sanitizer to HK and China. ( read more )..... Closed
10-00093 India company needs Quality Consultant for Quality Assurance Training needed for the quality auditing, in brief with respect to QA and regulatory ( read more )..... Closed
10-00089 Italy pharmaceutical manufacturer needs regulatory consultant for regulatory services for pharmaceuticals ( read more )..... Closed
10-00087 Regulatory Consultant needed by Austria Pharmaceutical Company for Reimbursement application to Slovakian Ministry of Health for an EMA registered Orpahn Drug ( read more )..... Closed
10-00085 Middle East Regualtory Consultant needed to advie on the regulatory norms for import of Sunscreen UVA/UVB products from Australia. Can the products approved by TGA and readily sold in Australia be imp ( read more )..... Closed
10-00084 INDIA EXCIPIENT MANUFACTURER NEEDS PHARMACEUTICAL CONSULTANT TO ADVISE OF US FDA REGULATION AND EC DIRECTIVE AMENDMENT: NEW US REGULATION RELATED TO FOOD & DRUG FOR EXCIPIENT ( GELATIN & CELLULOSE CA ( read more )..... Closed
10-00082 Pharmaceutical Regulatory expert needed for NDA and drug monograph submissions for a natural product. ( read more )..... Closed
10-00078 India Pharma needs Regulatory Consultant for FDA ANDA Submission, Regulatory fillings ( read more )..... Closed
10-00077 California Pharmaceutical Corp needs regulatory Consultant for FDA ANDA submission and OTC ANDA submission. ( read more )..... Closed
10-00071 Swiss based MNC manufacturing products in india seeks consultancy services for generic drug product registration in above mentioned countries. please revert with fee details. ( read more )..... Closed
10-00067 FDA Consultant needed for label review ( read more )..... Closed
10-00065 Central Laboratory specializing in clinical trials needs consultant to assist them in moving towards clinical diagnostic in support Pharma companies biomaker development. We would like to get a quote ( read more )..... Closed
10-00056 India Regulatory Consultant needed for pharmaceutical factory inspection ( read more )..... Closed
10-00055 India Regulatory Laboratory needed for Pharmaceutical Regulatory Filings ( read more )..... Closed
10-00053 Regulatory Consultant needed for Product registration ( read more )..... Closed
10-00048 Pharmaceutical company needs FDA regulatory affairs consultant to help decide on database lock date for Phase III trial (from a regulatory perspective) and to lead engagement with the FDA for upcomi ( read more )..... Closed
10-00047 New York pharmaceutical company needs regulatory consultant to advise on regulatory import and export. ( read more )..... Closed
10-00042 Saudi Arabia Pharmaceuticals Laboratory needed for validation consultant needed for validation consulting ( read more )..... Closed
10-00041 Regulatory Consultant needed to Support investigation of new drug for potential NADA FDA application. ( read more )..... Closed
10-00040 Government needs regulatory auditor to assist on good inspection practice of pharmaceutical warehouses (importers and wholesalers), post market surveillance ( read more )..... Closed
10-00037 INDIA PHARMACEUTICAL MANUFACTURER NEEDS PHARMACEUTICAL REGULATORY CONSULTANT FOR FDA SUBMISSIONS AND EUROPEAN COMMON TECHNICAL DOCUMENT EU CTD ( read more )..... Closed
10-00036 MIDDLE EAST BASED REGULATORY CONSULTANT TO ADVISE ON PHARMACEUTICAL REGULATORY PROCESS ( read more )..... Closed
10-00033 Biotech company needs Regulatory Consultant for all activities related to US and International regulatory compliance for investigational and approved drug. includes keeping all reporting and complianc ( read more )..... Closed
10-00031 India Regulatory Consultant and authorised agent needed to register a pharmaceutical product (drug) in India through Marketing Authorisation Holder (MAH) for a pharmaceutical product in India. My unde ( read more )..... Closed
10-00030 Asia based regulatory consultant needed to advise on regulatory requirements for Regulatory submissions in Japan ( read more )..... Closed
10-00027 Regulatory consultant needed with experience in regulatory filing and importing of veterinary pharmaceuticals into Mexico to assist with registration. ( read more )..... Closed
10-00024 Africa based consultant needed for assistance in finding the names of the various government regulatory agencies in Africa e.g Ghana, Kenya, Togo, South Africa etc. ( read more )..... Closed
10-00023 Consultant needed for FIM trial (2 sites, appx. 50 pts)of new dermal filler. Consultant will help with country and site selection, and lead process for getting clearance to conduct investigational tri ( read more )..... Closed
10-00020 USA ISO, GLP, GCP, ASQ certified auditor needed for pre-clinical and clinical bioanalytical laboratory (Method validation, Sample Analysis)and quality systems that support these activities." ( read more )..... Closed
10-00015 Compounding pharmacy needs internationally oriented regulatory affairs pharmaceutical consultant to advise them on going global ( read more )..... Closed
10-00012 Puerto Rico resident registered agent needed to file license applications/product listings in Puerto Rico ( read more )..... Closed
10-00011 Pharmaceutical Consultants needed for Pharmacovigiliance - Literature Searches for 50 products. 1) perform literature searches, with the aim to ensure that the adverse event reports from the local ( read more )..... Closed
10-00010 Middle East Regulatory Consultant needed for Facility Design and Saudi FDA approval ( read more )..... Closed
10-00008 Employee in the Clinical Trial Unit of Biotechnology Regulatory Affairs Department needs Training on regulatory aspects of biotechnology products. ( read more )..... Closed
10-00007 India Pharmaceutical company needs advice on validation of DPT tunnel Question is: What are the Actual time exposures for Vial to depyrogenate , is it depend o Belt length? ( read more )..... Closed
10-00006 Experienced Pharmaceutical Consultants needed to file an NDA application in Russia. ( read more )..... Closed
10-00004 Pharmaceutical Regulatory Consultant needed to determine FDA regulatory filing requirements, liaise with the FDA, guide document filing. ( read more )..... Closed
10-00003 Pharmaceutical Regulatory consultant needed for assistance to submit a duplicate application to Algeria Authorities ( read more )..... Closed
09-0185 Pharmaceutical manufacturer needs Africa Regulatory Consultant to handle all regulatory matters involving facility registration in african countries, dossiers preparation etc. On urgent basis facility ( read more )..... Closed
09-0184 Pharmaceutical Regulatory Consultant needed for Japan PMDA/MHLW drug master file registration ( read more )..... Closed
09-0180 Biotech Manufacturer needs Turkey Consultant or Qualified Person for filing of dossiers of few products in turkey. ( read more )..... Closed
09-0177 India Pharmaceuticals mfg needs regulatory consultant for Turkey MOH,Uk-MHRA and AUTGA and Afssaps MCC south Africa and Health Canada Approvals ( read more )..... Closed
09-0164 Legal Counsel needs Pharmaceutical Regulatory Consultant with FDA and Health Canada regulations expertise. We are legal counsel for a company who is currently involved in litigation where there may be ( read more )..... Closed
09-0162 Pharmaceutical Company requires Regulatory Consultant to assist with GMP requirements and compliance for proposed new sterile fill and tabletting operation for clinical trials ( read more )..... Closed
09-0159 Regulatory Consultant with US and China regulatory consultants needed for FDA GMP audits and monitor compliance of a pharmaceutical plant in China. We have a project to buy a pharmaceutical API from C ( read more )..... Closed
09-0157 Malaysia Mfg needs Regulatory FDA Consultant for FDA Product registration, labeling and fulfilling FDA product registration requirement ( read more )..... Closed
09-0154 Pharmaceutical Company needs Canada Regulatory Consultant to advise on Importing Pharmaceuticals from Poland. ( read more )..... Closed
09-0152 Consultant needed to advise on regulatory co-development strategies for a new oncology drug and in-vitro diagnostic for a genomic biomarker ( read more )..... Closed
09-0149 Large, Multinational Pharmaceutical Company needs FDA Consultant for filing GMP FDA annual report ( read more )..... Closed
09-0148 FDA CONSULTANT NEEDED FOR LABELING REVIEW ON COSMETICS, OTC DRUGS. PACKING REVIEW ALSO. ( read more )..... Closed
09-0147 Regulatory Consultant needed for Compliance with Canadian legislation for importation of food and pharmaceutical ingredients, additives, etc ( read more )..... Closed
09-0146 Large Pharmaceutical Company needs Regulatory Consultant to for US FDA CMC - Annual Reports. Working with various internal operations groups in order to summarize reportable changes for the year. Onli ( read more )..... Closed
09-0145 Large Cairo pharmaceutical organization needs EMEA, FDA GLP/GCP Consultant to ensure compliance of bioequivalence & Pharmacokinetic research centre complying with regulatory associations, EMEA, FDA. I ( read more )..... Closed
09-0143 Prague Company needs Regulatory Consultant for Product filling and fees arrangements in Slovenia. We are planning for submission of our product in Slovenia, need help to arrange communication with the ( read more )..... Closed
09-0139 Central Supply Chain in EU needs a regulatory consultant to provide advice regarding supplying a licensed product in Switzerland ( read more )..... Closed
09-0135 Singapore contact lens company seeking consultant to register product in Indonesia. Indonesia importer is available already. ( read more )..... Closed
09-0132 Seeking consultant or local rep to register contact lens product in Saudi Arabia ( read more )..... Closed
09-0131 FDA Consultants needed for helping solve cGMP issues in drug product & API manufacturing: Facilities & Equipment Design/Environmental Control/manufacturing practices, Cleaning/Cleaning Validation, Cha ( read more )..... Closed
09-0127 Consultant required to help import an inhaler from Thailand to the USA that consists of ingredients menthol,eucalyptus and camphor. It is a 2 part product- inhaler for nose and ointment for skin, and ( read more )..... Closed
09-0125 Regulatory consultant needed with experience in regulatory filing and importing of veterinary pharmaceuticals into Chile. ( read more )..... Closed
09-0124 Singapore Pharmaceutical Company needs Regulatory Consultant for Saudi Arabia Health Authority Regulatory submission for drug registration ( read more )..... Closed
09-0122 Russian pharmaceutical company needs a regulatory consultant to register its drugs and active substances with FDA and EMEA and advise on import strategy. ( read more )..... Closed
09-0120 Need Consultant for EU and US ANDA submissions ( read more )..... Closed
09-0117 Pharmaceutical Regulatory Consultant needed for Endocrine Phase IIa Clinical Trial for IND orphan drug designation ( read more )..... Closed
09-0110 Looking for Regulatory consultants to represent our company ( read more )..... Closed
09-0107 Asia Regulatory COnsultant needed for registering generic opthalmic product in S Korea ( read more )..... Closed
09-0101 European Union Pharmaceuticals Consultant needed for EU gap analysis, filing communication and translation services ( read more )..... Closed
09-0098 Middle East Based Consulting Firm needed to Develop and maintain regulatory activity module in the middle east ( read more )..... Closed
09-0095 Quality Consultant needed for Quality Systems, SOP Writing, Training ( read more )..... Closed
09-0094 Clinical Trial Consultant needed for regulatory support for clinical trial application, name patient programs, interactions with Health Authorities. ( read more )..... Closed
09-0093 Pharmaceutical Manufacturer needs Regulatory Consultant for European Drug Master File (EDMF) or Active Substance Master File (ASMF) ( read more )..... Closed
09-0091 Russia Patented, Antiviral Biopharmaceutical manufacturer US patent office needs FDA Regulatory Consulting Firm to assist in FDA marketing authorization. ( read more )..... Closed
09-0090 Europe Pharmaceutical Company requires Pharmaceutical Regulatory Consultants for DMF preparation and filing ( read more )..... Closed
09-0089 Pharmaceutical Company needs Technical consultant for a project setting up warehouse for pharmaceuticals in cairo ( read more )..... Closed
09-0085 Clinical Trial Auditor needed for auditing a Pharmaceutical Clinical Trial ( read more )..... Closed
09-0084 FDA consultant needed for Consultation on FDA guidelines for brand promotion during the prelaunch market conditioning period-2 years prelaunch of product ( read more )..... Closed
09-0082 Regulatory Consultants needed to advise on requirements for Montenegro pharmaceutical DMF submission ( read more )..... Closed
09-0081 Pharmaceutical Mfg needed FDA Consultants for FDA ANDA submission for injectable ( read more )..... Closed
09-0080 Pharmaceutical Mfg needs qualified ANVISA consultant to audit CRO for BE/BA studies for ANVISA (Brazil) ( read more )..... Closed
09-0079 Middle East Quality Consultants needed for Quality Assurance Development and Product Development ( read more )..... Closed
09-0078 Pharmaceutical manufacturer needs Pharmaceutical Consulting Firm for cGMP training ( read more )..... Closed
09-0074 Regulatory Consulting firm in the middle east region particularly for UAE, Kingdom of Saudi Arabia is required ( read more )..... Closed
09-0066 Large Corporation needs FDA Consultant for training/mock FDA inspections with primary focus being enforcement of the Post Marketing Adverse Drug Experience Reporting Regulations. ( read more )..... Closed
09-0063 Ireland Pharmaceutical Company needs Language Translator for Translations for SPC, PIL and labeling ( read more )..... Closed
09-0061 Pharmaceutical Mfg needs Regulatory Consultant for assisting on FDA submission ( read more )..... Closed
09-0058 Pharmaceutical company needs Asia Regulatory Consultant to advise on KDA autorization to sell pharmaceuticals to South Korea. We need regulatory affairs services in KFDA for market authorization. ( read more )..... Closed
09-0057 Life Science Mfg needs Asia Regulatory Consultant for market entry and claims strategy for foreign herbal products to sell in Japan, China and S Korea. ( read more )..... Closed
09-0055 Small pharmaceutical manufacturer requires regualtory assistance in converting paper-based DMF's to eCTD format. ( read more )..... Closed
09-0054 What type of cerification or validation requirements exist for Labeling Equipment Manufacturers in the Pharmaceutical industry? ( read more )..... Closed
09-0051 Pharmaceutical Regulatory Consultant needed to assist pharmaceutical mfg in complying with FDA requirements for ink on foil packaging for the pharmaceutical industry. ( read more )..... Closed
09-0044 Pharmaceutical Regulatory Consultant needed to review OTC drug labels and make sure they are compliant with the FDA's OTC drug labeling requirements. ( read more )..... Closed
09-0039 US FDA Pharmaceutical Consultant needed for fda registration approval to operate a warehouse and distribution site for pharmaceutical product handling ( read more )..... Closed
09-0037 "Pharmaceutical Regulatory consultants needed for dossier submission in Mexico, Canada and Latin America Region. ( read more )..... Closed
09-0035 Experienced FDA Regulatory Consultant needed to assist on FDA pharmaceutical regulatory submissions. ( read more )..... Closed
09-0029 Pharmaceuticals Regulatory Consultant needed for Global project related to re-Positioned compounds and their formulations and regulatory requirements around these in different jurisdictions ( read more )..... Closed
09-0027 Large Pharmaceutical Manufacturer needs Pharmaceutical Validation Consultant needed to help us understand the FDA requirements for cleaning of parenteral manufacturing equipment. When is it required t ( read more )..... Closed
09-0026 US Pharmaceutical Manufacturer needs Pharmaceutical Consultant to provided FDA regulatory help with OTC pharmaceutical filing, labelling, review, approval, labelling requirements and other issues re ( read more )..... Closed
09-0024 Canada pharmaceutical chemical manaufacturer needs FDA GMP consultant to perform GMP gap analysis for the pharmaceutical chemicals it sells to pharmaceutical manufacturers. ( read more )..... Closed
09-0017 Pharmaceutical Company needs good technical and medical writers to prepare a MAA as together we finalize out a simultaneous NDA. ( read more )..... Closed
09-0015 India Export Manufacturer needs regulatory consulting firm to assit in ANVISA approval for manufacturing plant located in India. ( read more )..... Closed
09-0010 Pharmaceuticals manufacturer needs Quality Consultant needed to implement lean manufacturing, six sigma principles. ( read more )..... Closed
09-0001 Regulatory Consultant experienced in advising on Pharmaceutical Product Import which is exported from Singapore to India ( read more )..... Closed
08-0174 Pharmaceutical Manufacturer exploring the possibility of a FDA GMP audit of an API manufacturing facility in Germany. Auditor must speak, read and write German and English. ( read more )..... Closed
08-0173 Pharmaceutical Legal or Regualtory Consultant needed to prepare a written regulatory opinion, outlining the regulatory path requirements and time-line to obtain marketing approval for topical product ( read more )..... Closed
08-0170 INDIA PHARMACEUTICAL MANUFACTURER NEEDS REGULATORY PHARMACEUTICAL CONSULTANT TO ADVISE ON REGISTRATION REQUIREMENTS ( read more )..... Closed
08-0169 Regulatory Pharmaceutical Consultant needed to advise on Timeline specifications for ANVISA GMP Inspections ( read more )..... Closed
08-0168 Regulatory Consultant needed for advising on compliance of core label and Informed Consent Forms. For instance what is the difference between proof of concept, proving efficacy. Does FDA requires Info ( read more )..... Closed
08-0163 Pharmaceutical Regulatory Consultant needed to advise on generic pharmaceuticals in Russia ( read more )..... Closed
08-0162 Pharmaceutical regulatory consultant needed in India ( read more )..... Closed
08-0160 Pharmaceutical Manufacturer needs Regulatory Consultant for Summary of Product Characteristics (SPC) from Austria and also need to procure samples for development purpose from all Scandinavian countri ( read more )..... Closed
08-0158 Laboratory Consultant needed to provide Compliance Training in microbiology methods in pharmacential industry ( read more )..... Closed
08-0157 Pharmaceutical Manufacturer needs Pharmaceutical Consultant for Drug manufacturing plant setup ( read more )..... Closed
08-0155 Dermatology Company needs FDA and EMEA Regulatory Consultant for Strategic guidance and drug filing services is required in India for an international pharma company, which develops topical gel and to ( read more )..... Closed
08-0151 Swiss company needed that can take over a MAH for a product while the US-based owner finds a new marketing partner. The product will be taken off the market for the duration of this need, so little wo ( read more )..... Closed
08-0149 Regulatory Consultant needed in Jordan which can give the regulatory service (compile the Dossier as required by JOrdan FDA, submit & follow up the Dossier with JOrdan FDA. Obtain the registration app ( read more )..... Closed
08-0146 FDA Pharmaceutical Regulatory Consultant needed to help us with ANDA filing with US FDA, ( read more )..... Closed
08-0141 Consultant needed to advise on compliance with United Kingdom regulators regarding labelling and ingredients. ( read more )..... Closed
08-0140 Pharmaceutical consultants needed for FDA pharmaceutical registration service in india. ( read more )..... Closed
08-0132 Pharmaceuticals Regulatory Consults needed to assist in product development related to NCE (New chemical entity) and apply that to the medical devices we are currently developing. Therefore we want to ( read more )..... Closed
08-0130 European pharmaceuticals company that is acquiring 3 prescription drugs needs US FDA registered agent. They presently have no US legal entity, and require FDA registered agents for the establishment l ( read more )..... Closed
08-0128 Biopharmaceutical manufacturer needs Bippharmaceutical Consultant to assist in launch of pharmaceuticals to Turkey. Need consultant about regulatory affairs and licensing. ( read more )..... Closed
08-0126 Pharmaceutical Regulatory Consultant needed to assist India Pharmaceutical Manufacturer on Format used for Dossier in Common Technical Document CTD format for Brazil ( read more )..... Closed
08-0125 EU PHARMACEUTICAL REGULATORY CONSULTANT NEEDED TO ASSIST ON GUIDELINES AND REQUIREMENTS OF eCTD FILING . ( read more )..... Closed
08-0121 India pharmaceutical company planning to submit applications for approval from MHRA, MCC & TGA are seeking competent Regulatory Consultants to assist us in successfully file our applications. ( read more )..... Closed
08-0120 Generic Drug Manufacturer in INdia needs US FDA Agent for Pharmaceutical Drugs. ( read more )..... Closed
08-0119 Pharmaceutical Quality Consultant needed in Saudi Arabia to design quality assessment program which cover the following points:  The requirements of the quality part of the dossier based on the CTD ( read more )..... Closed
08-0114 Pharmaceutical Manufacturer needs regulatory consultant base in Saudi Arabia to help in conduct Clinical Trial and Registration of chemical drugs ( read more )..... Closed
08-0108 German based Global Operating Pharmaceutical Company needs Pharmaceutical Regulatory Consultants for filing generic drug application in Japan ( read more )..... Closed
08-0107 Pharmaceutical Regulatory Consultants needed to help overseas manufacturing companies file CTDs to the Phillipine s regulatory agency. ( read more )..... Closed
08-0099 Large Pharmaceutical Manufacturer needs Pharmaceutical Regulatory Consultant with experience on oncology drug development to discuss the regulatory strategy. ( read more )..... Closed
08-0098 Biotechnology Life Science Company needs Pharmaceutical Regulatory Consultant in India ( read more )..... Closed
08-0097 Pharmaceutical Regulatory Consultants needed for assisting on preparing a US FDA ANDA for a new product to the FDA. ( read more )..... Closed
08-0096 FDA Quality Consultant needed to review existing Quality system and prepare for a re-inspection by the FDA ( read more )..... Closed
08-0091 Experienced Regulatory Consultant needed to provide regulatory guidance on shelf-life and labeling requirements of Prescription Medical Foods along with a potential to help on other issues. ( read more )..... Closed
08-0085 Regulatory Consultant/Sterilization Expert needed who understands the sterilization landscape, specifically someone who understands the FDA Warning letter sent to Steris on their Steris System 1. ( read more )..... Closed
08-0084 Regulatory Consultants needed with experience in Part 11 compliance and computer system validation ( read more )..... Closed
08-0083 Pharmaceutical Regulatory Consultants with experience in US IND Maintenance needed to introduce Change Control Procedures (CCP) to R&D line functions to assure compliance with the requirements at 21CF ( read more )..... Closed
08-0076 Consultant for regulatory approval for the Pharmaceutical Formulation Products in overseas contraries. [Particularly African countries]Country wise requirement of the manufacturing setup and product ( read more )..... Closed
08-0074 Pharmaceutical Regulatory Consultant needed to conduct initial GMP/GLP mock inspection, advice on corrections necessary to ensure FDA approval, and then submission of ANDA for a generic drug. ( read more )..... Closed
08-0071 Regulatory consultant needed to advise and file registrations for OTC drugs in the Caribbean ( read more )..... Closed
08-0068 Pharmaceutical Manufacturer needs pharmaceutical regulatory consultant for submission of a drug dossier to the Brazilian Health Authorities ( read more )..... Closed
08-0067 Pharmaceuticals Regulatory Consultant to advise re: CTD in Saudi Arabia, South Africa, Spain, Australia, for an herbal topical application for wound healing. What are the regulatory requirements? Do w ( read more )..... Closed
08-0060 Regulatory consulting services required for drug registration,Finding summary of product characteristic ( read more )..... Closed
08-0059 Pharmaceutical regulatory consultants needed for product registration by DCP, importing samples ( read more )..... Closed
08-0058 Pharmaceutical Regulatory Consultants in European countries required ASAP ( read more )..... Closed
08-0054 Regulatory consultant needed to advise on pharmaceutical submissions ( read more )..... Closed
08-0048 Experienced US FDA consultant needed that is familiar with putting together a De Novo or ANDA specifically for anti-microbial hand soaps for a suite of 3 proven anti-microbial handsoaps and rubs that ( read more )..... Closed
08-0045 US FDA Regulatory consultant needed to assist in Registration of Natural Products, Cosmetics and an OTC pharmaceutical with US Food and Drug Administration. ( read more )..... Closed
08-0044 Regulatory Consultant specializing in China needed to for IDL to launch generic pharmaceutical products in China ( read more )..... Closed
08-0042 Regulatory Consultant needed to advise on equilvalent of the US FDA 1572 and delegation forms in Germany ( read more )..... Closed
08-0040 Quality Systems consultant needed for quality system development in clinical trials and pharmacovigilance. ( read more )..... Closed
08-0039 Regualtory consultant needed to provide a detailing of the prevailing legislative / regulatory requirements governing labor relations and workforce shceduling in SPain and Italy. Should include a comp ( read more )..... Closed
08-0036 WHO GMP Pharmaceutical Manufacturers needs pharmaceutical regulatory consultant to go for USFDA approval of our Manufacturing plants and register both OTC & Generic Formulations. ( read more )..... Closed
08-0031 Pharmaceutical regulatory consultant needed to help with pharmaceutical US FDA ANDA Submission ( read more )..... Closed
08-0029 Regulatory Consultant needed for consulting on a veterinary pharmaceutical already licensed in Poland. We require assistance in preparing the renewal application and also in updating the dossier for t ( read more )..... Closed
08-0028 Regulatory Consultant needed for consulting / gap analysis for EU GMP compliance for veterinary vaccines. ( read more )..... Closed
08-0026 Law Firm looking for an expert witness and/or consultant to assist us in a case in federal court involving the manufacture of lutein by one company that was then sold to another company which incorpo ( read more )..... Closed
08-0024 Audit of two central labs in Argentina (Buenos Aires) and two central labs in India (Ahmedabad and Bangalore). ( read more )..... Closed
08-0023 Regulatory consultants needed for GMP, FDA & EU submissions ( read more )..... Closed
08-0020 Pharmaceutical manufacturer needs EMEA regulatory consultant to provide expertise in evaluating existing manufacturing facility and advise on actions to achieve compliance with EMEA regulations. ( read more )..... Closed
08-0015 Experienced FDA consultant neeeded for consultancy on setting-up an FDA compliant Pharma manufacturing unit ( read more )..... Closed
08-0014 Regulatory Consultant needed for a summary of product charecteristics for a single product for Poland. ( read more )..... Closed
08-0013 Pharmaceuticals Regulatory Consultant needed to determine if it is feasible to extend plans for a trial into Belize, Costa Rica, Dominican Republic, and Virgin Islands. We need to know how long it wil ( read more )..... Closed
08-0005 Local representative regulatory consultant needed for pharmaceutical marketing authorizations in Bulgaria, Croatia, Serbia, Montenegro, Bosnia Herzegovina and Macedonia. ( read more )..... Closed
08-0004 Attorney representing a pharmaceutical company in a dispute with a manufacturer here in the Superior Court of San Diego County. I am interviewing potential expert consultants/witnesses to provide tes ( read more )..... Closed
08-0003 FDA Pharmaceutical Regulatory Consultant needed for ANDA preparation and submission. Consultant must have experience with FDA and must have been successful on gaining approval on FDA submissions. ( read more )..... Closed
08-0002 Urgent 3 month need for experienced Japanese Consultants (x2)to assist with a Global Compliance project Post-approval Compliance - Japanese Regulations & Directives expertise. GMP, CMC & compliance e ( read more )..... Closed
08-0001 Regulatory consulting company needed to represent a combination product manufacturer company with the US FDA DURING THE DEVELOPMENT PLAN. We have submitted IND. Experts needed in combination products ( read more )..... Closed
07-0145 Regulatory consultant needed for providing points of view on audit ( read more )..... Closed
07-0141 European Union Regulatory Affairs consultant needed for support is needed for the following Eastern European Member States: Bulgaria, Slovakia, Slovenia, Lithuania, Latvia, Poland, Hungary, Estonia, C ( read more )..... Closed
07-0140 CRO offering BA/BE services to generic pharma companies needs consultant to assist in applying for ANVISA (Brazil) certification of our centre ( read more )..... Closed
07-0139 Regulatory consultant needed who speaks Slovak and English to attend a client affiliate site and collect several licensed dossiers. Products include Pharmaceutical, Nutritional, Consumer Health and V ( read more )..... Closed
07-0138 Regulatory Consultant needed to assist in notifying Spanish authorities of product recall ( read more )..... Closed
07-0137 Engineering firm needed for developing FDA GMP approved pharmaceutical manufacturing plant on toll basis for a US company. The plant will be designed as per requirement of the US company. ( read more )..... Closed
07-0136 Pharmaceutical Company needs consultant for developing regulatory strategy for Europe, gUIDENCE FOR SELECTION OF RMS AND CMS, DOSSIER REVIEW AND GUIDENCE, EXPERT REPORT ( read more )..... Closed
07-0135 Pharmaceutical clinical trial consultant needed for developing FDA GCP clinical trial for new drug rimonabant ( read more )..... Closed
07-0134 Leading Global Pharmaceutical Organisation urgently require an on-site Regulatory Affairs Executive in Istanbul, to cover an employee secondment for 6 months. You must have experience of variations & ( read more )..... Closed
07-0132 Pharmaceutical regulatory consultant needed for Mock US FDA Inspection for an API manufacturer in JAPAN is needed. The client has prepared for a forthcoming FDA inspection for years, and is confident ( read more )..... Closed
07-0122 Pharmaceutical Regulatory Consultant needed to assist in setting up a pharmacovigilance system based on international best practice ( read more )..... Closed
07-0120 Seasoned CMC Pharmaceuticals Regulatory professional(s) to prepare the CMC sections of regulatory license files. ( read more )..... Closed
07-0119 Pharmaceutical Regulatory Consultant needed for regulatory project for liquid foundation with SPF 15 actives. ( read more )..... Closed
07-0118 Pharmaceutical Regulatory Consultant needed for Management and Preparation of ANDA for an inmediate release tablets drug product using the CTD format. To be submitted to US, and subsequently to EU ( read more )..... Closed
07-0116 Need management services for completion of EPA registration of disinfectant product. After completion of EPA registration, will need to manage all FDA required tests and studies needed for approval o ( read more )..... Closed
07-0115 Regulatory consultant needed to register medicated topical hormone gels in Mexico. Require liason and local contact to do the necessary work. ( read more )..... Closed
07-0114 USFDA Regulatory Consultant needed for consulting on USFDA audit ( read more )..... Closed
07-0113 Regulatory consultants needed to provide regulatory strategy and approval pathway for switch from approved iv formulation to an oral formulation. Prior successful experience in this area preferred. ( read more )..... Closed
07-0107 Consultant in regulatory affairs is needed for small drug development company to advise on regulatory paths with the fixed dose combination drugs. Vancouver (BC) or Seattle areas are prefered. ( read more )..... Closed
07-0106 Regulatory consultant needed for consulting for cancer drug ( read more )..... Closed
07-0104 Vendor required to perform label comprehension study for OTC drug ( read more )..... Closed
07-0101 Regulatory consultant needed to provide training programmes for ectd submissions ( read more )..... Closed
07-0099 Regulatory consultant needed for advising on guidelines to be followed for registration of API with ANVISA, Brazil. ( read more )..... Closed
07-0095 Regulatory consultant needed to aid in the filing of a Drug Master File in Japan. The DMF has already been filed in the US in the CTD format. ( read more )..... Closed
07-0089 Pharmaceutical consultant needed to represent client at MOH meetings, discuss optimal strategy for registration of pharmaceuticals with MOH;hands on activities with respect to dossier compilation and ( read more )..... Closed
07-0088 Regulatory consultatnt needed for assistance with obtaining regulatory approval in Korea. Our products is cleared by FDA and health Canada. Also CE marked. ( read more )..... Closed
07-0085 Contract Manufacturer of pharmaceutical packaging needs FDA regulatory consultant to audit processes for FDA Good Manufacturing Practices GMP. ( read more )..... Closed
07-0081 Pharmaceutical regulatory consultant needed to assist in understanding of exact regulatory process for applying for and obtaining marketing authorization and approval ( read more )..... Closed
07-0079 Pharmaceuticals manufacturing company needs pharmaceuticals regulatory consultant to assist with registering products in the USA. ( read more )..... Closed
07-0077 Pharmaceutical consulting firm needed for development of nasal(aerosol) department ( read more )..... Closed
07-0075 Regulatory consultants needed for selection of RMS/CMS meeting request and preparation. MAA consulting and review ( read more )..... Closed
07-0074 Large pharmaceuticals company needs validation consulting company for qualification/validation services in support of the Protein Therapuetics Development qualification/validation program. These serv ( read more )..... Closed
07-0073 Generic Pharmaceutical Manufacturer needs registration and approval consulting for Active Ingredients and Finished Dosage Forms in Japanese market. In this connection we would like to know the sched ( read more )..... Closed
07-0072 Pharmaceuticals consultant wanted for general preclinical (tox & DMPK)and regulatory consulting ( read more )..... Closed
07-0071 Manufacturer of HDPE bottles needs an FDA pharmaceutical consultant who can file USFDA Drug Master File and get vendor approval for from us fda. We prefer consultant from india ( read more )..... Closed
07-0069 Pharmaceuticals Regulatory Consultant needed to assist in filing an US FDA Drug Master File (DMF) ( read more )..... Closed
07-0065 Clinical Quality consultant needed to provide GCP Audit Training in QA Good Clinical Practices Auditing on study site for pharmaceutical CRO ( read more )..... Closed
07-0064 Clinical Trial COnsultant needed for setting up Pharmaceutical Clinical Trials in Romania. ( read more )..... Closed
07-0058 Pharmaceutical consultant needed to provide insightful FDA GMP training with actual field experiences. Up and coming pharmaceutical company with rapid growth needs compliance training for entire (smal ( read more )..... Closed
07-0057 Regulatory Consultant needed to register pharmaceutical manufacturer in middle east. ( read more )..... Closed
07-0050 Regulatory consulting firm needed for filing an application for a generic drug ANDA application ( read more )..... Closed
07-0046 Assistance in preparation of USFDA DMF submission for pharmaceutical raw material, GMP assistance and audit preparation for USFDA audit. ( read more )..... Closed
07-0040 Pharmaceutical, manufacturing and trading company needs consultant needed for combination dossier supply for the injection form "FENPIVERINIUM BROMIDE + METAMIZOLE SODIUM + PITOFENONE" . ( read more )..... Closed
07-0033 Pharmaceuticals Consulting Firm needed for Fast track approval or orphan drug approval. Drug registration approval in country specified. Import of unregistered drug in those countries. ( read more )..... Closed
07-0029 Regulatory consultant needed for UK MHRA approval for our pharmaceutical formulation manufacturing unit. ( read more )..... Closed
07-0026 Small formulations company needs Pharmaceuticals Regulatory Consultant for consulting on DESI products ( read more )..... Closed
07-0024 Pharmaceuticals Regulatory Consultant needed for assisting on MHRA approval for pharmaceutical preparations plant. ( read more )..... Closed
07-0018 Consultant needed for certification training courses related to international regulatory guidelines ( read more )..... Closed
07-0016 Manufacturer of FDG radioisotopes needs validation consultants to guide them and validiate this unit ( read more )..... Closed
07-0015 Consultant needed for compliance review of label for an OTC aloe products and aloe juice drink to ensure that labels are compliant with FDA and Texas Departement of State Health Services. I need to ( read more )..... Closed
07-0014 Clinical Consultant needed for clinical trials training in pharmaceuticals,medical devices,cosmetics,food and beverages ( read more )..... Closed
07-0013 Pharmaceuticals Consultant needed for the assistance on the development and submission of new labelling for new pharmaceutical products based on existing approved ANDA's. ( read more )..... Closed
07-0011 Dental manufacturer needs regulatory consultant to advise on regulatory restrictions on Dental Health Products.( Mouth Rinse, Whitening and Xylitol) ( read more )..... Closed
07-0010 Consultant expeireinced in the manufacturing of biopharmaceutical products made in cell culture needed for extensive market research on the market of powder media with the goal to set up a state-of th ( read more )..... Closed
07-0009 Company has a cGMP API and wants to develop a portfolio of formulation opportunities to evaluate ( read more )..... Closed
07-0008 Industrialist that has set up a pharmaceutical manufacturer needs building under constuction needs consultant to assist on having it approved/inspected by FDA. ( read more )..... Closed
07-0007 Pharmaceuticals chemical manufacturer needs consultant to advice on the exact compliance requirements and certification procedures for Nutraceutical APIs and Drug products. ( read more )..... Closed
07-0004 Pharmaceuticals company needs regulatory consultant to provide comprehensive product-registration services and requirements right from product development , registration and regulatory approval of pha ( read more )..... Closed
07-0003 Consultant needed for advice on performing preclinical toxicology and first-in-man studies on inhalational drug in South Africa or Brazil ( read more )..... Closed
06-0176 Consulting needed on rquirements for setting up API plant for oncology medicines phase 3 in India ( read more )..... Closed
06-0174 Consultant needed to advise on GLP,NABL,GMP and how it is applied including to upgrading of diagnostic procedures. ( read more )..... Closed
06-0172 Consultant needed for Dossier preparations for regulated markets, certifications & Technical reviews ( read more )..... Closed
06-0169 Consultant needed to inspect three pharmaceutical manufacturing areas for cGMP compliance. Two locations in Huntsville, AL and One in Charlotte, NC ( read more )..... Closed
06-0167 Regulatory consulting services for drugs and biotech to assist a small specialty pharma company. ( read more )..... Closed
06-0165 Pharmaceutical e-marketing regulatory information on 19 countries-- beginning with Germany, Spain, UK. ( read more )..... Closed
06-0164 Independent consultant needed with at least 5 years experience in software/computer systems validation in a GMP environment, preferably medical device manufacturing. ( read more )..... Closed
06-0163 Consultant needed for development of EU- GMP system for pharmaceutical manufacturing facility. From Gap analysis till the achievement of EU-GMP. ( read more )..... Closed
06-0162 Consultant needed to conduct audits of clinical trial centres, TMF's ,related systems etc. to ICH GCP standards ( read more )..... Closed
06-0155 21 CFR Part 11 consultant needed for GAMP training & review of MES package to ensure it complys with 21CFRpart11. Would also like basic GAMP 4 training for 5 staff ( read more )..... Closed
06-0154 Agency in western part of India who can authorise and train us to acclaim DMF and MHRA certification for supply of packaging material co-extruded 3 layer poly film for packing of IV Solutions required ( read more )..... Closed
06-0152 GMP consultant needed to support a Japanese company in cGMP regulations in preparation for a pre-approval inspection PAI ( read more )..... Closed
06-0151 Pharmaceutical Regulatory Consultant needed for consulting on a Drug Master Filing (the Cost and feasibility of filing DMF) ( read more )..... Closed
06-0150 Consultant needed for due dilligence in feasibility of conducting a Phase 3, oncology study in India, Japan, and Australia. ( read more )..... Closed
06-0143 Regulatory consultant experienced in ANDA's needed with strong CMC experience with liquid pharmaceuticals needed for several ANDA supplements and also a product transfer. This will be a 6-8 week full ( read more )..... Closed
06-0138 Validation consultant needed for software validation as per 21cfr standards. ( read more )..... Closed
06-0137 Regulatory consultant experienced with FDA importation of 10 animal drugs into the US needed. Spanish speaking consultant preferred. ( read more )..... Closed
06-0135 Pharmaceuticals manufacturer needs consultant for consulting on Canadian regulatory requirements i.e Audit requirements, dossier requirements and others ( read more )..... Closed
06-0127 FDA GMP pharmaceuticals training ( read more )..... Closed
06-0123 VERY REPUTABLE EUROPEAN PHARMACEUTICS MANUFACTURING CONSULTING COMPANY NEEDED FOR PROJECT IN MIDDLE EAST ( read more )..... Closed
06-0118 Regulatory consultant needed to guide cGMP manufacturing, process qualification, process validation, virus clearance validation to meet USFDA requirements. ( read more )..... Closed
06-0114 Pharmaceuticals consultants needed for prepartion of guidelines for cGmp inspections in every area of pharmaceuticals such as production of every dosage form including sterile preparations and Quality ( read more )..... Closed
06-0113 East Asia US FDA GLP and cGMP consultants needed for consulting to CRO's and pharmaceutical companies. The consultants should be physically located in East Asia or be available to be in East Asia for ( read more )..... Closed
06-0111 Regulatory consultant needed for Canada oncology New Drug Submission (NDS) NDS in TPD, Canada. ( read more )..... Closed
06-0110 Consultant needed for advising Dental Manufacturer on European registration processes for toothpaste with 1.1% neutral Sodium fluoride ( read more )..... Closed
06-0109 Consultant needed for advising on compilation of EU CTD Common Technical Document dossiers for vaccine/parenterals pharmaceuticals ( read more )..... Closed
06-0108 Consultant needed for preparation of pharmaceuticals product dossier in CTD format for drug registration in USA, UK & Japan ( read more )..... Closed
06-0106 Training on Method Validation as per FDA cGMP Good Manufacturing Practices and Calibration of Analytical Testing Equipment ( read more )..... Closed
06-0105 Pharmaceuticals manufacturer needs cGMP pharmaceutical regulatory consultant to prepare FDA pharmaceuticals ANDA for tablets and prepare facility for cGMP. ( read more )..... Closed
06-0104 Regulatory consultant experienced with combination products (medical devices/pharmaceuticals) approval process in the UK needed for providing outline of regulatory approval process. ( read more )..... Closed
06-0102 Sponsor needs consultants for preparing Annual Product Reports, Product Renewals and post-approval submissions in CTD format ( read more )..... Closed
06-0100 Expert pharmaceuticals consultant with specialization in sterile pharmaceuticals needed to provide opinion on pharmaceuticals with transdermal root of administration ( read more )..... Closed
06-0097 Pharmaceuticals Regulatory Consultant needed for assistance with EU Common Technical Document (EU CTD) and GMP ( read more )..... Closed
06-0095 Pharmaceuticals regulatory consultant wanted for US FDA ANDA approval of pharmaceutical tablets as well as preparation of GMP manufacturing facility. ( read more )..... Closed
06-0094 Manufacturers of pharmaceuticals hard gel capsules needs pharmaceutical regulatory consultant for european registration, auditing, and filing an EDMF for approval to market product in Europe. ( read more )..... Closed
06-0093 Pharmaceutical manufacturer needs a consulting firm that to assist in registering and licensing pharmaceutical products, preparing submissions and dossiers in multiple countries in Asia (Thailand,Viet ( read more )..... Closed
06-0092 Pharmaceutical regulatory consultants needed for assistance in compilation and filing of dossier submissions for registration of generic pharmaceuticals in Japan. Familiarity with Biostudies, English ( read more )..... Closed
06-0091 Regulatory consultant needed to consult on labeling regulatory requirements on pharmaceuticals used in clinical trials /studies in Egypt ( read more )..... Closed
06-0088 Pharmaceutical Regulatory Consultant needed for labeling reviews for pharmaceuticals products ( read more )..... Closed
06-0087 Regulatory consultant needed for assistance with Canada DIN and NHP product filing for items containing SPF ( read more )..... Closed
06-0086 Pharmaceuticals Manufacturer needs regulatory consulting for US FDA registration and preparation of ANDA. BA and BE inspections also required. ( read more )..... Closed
06-0078 Pharmaceutical manufacturer needs pharmaceutical regulatory consultant to guide them in US FDA audit and regulatory documentation matters. ( read more )..... Closed
06-0072 Regulatory consultant needed for assisting in e-Submissions across the globe including ANDA, NDA and BLS's. Also kindly let us know whether you have any tools to cater to the e-submissions for ANDA, N ( read more )..... Closed
06-0071 Regulatory consultant needed for preliminary consulting on documentation needed for FDA pharmaceutical New Drug Applications (NDA), EU Common Technical Documents (CTD), FDA GMP Audits for pharmaceutic ( read more )..... Closed
06-0064 Life Sciences company needs Validation Consultant for FDA Validation of LIS Software ( read more )..... Closed
06-0063 Pharmaceutical Regulatory Consultant needed for pharmaceutical product registrations in Russia ( read more )..... Closed
06-0062 Pharmaceutical Regulatory Consultant needed for assistance in filing US FDA ANDA on one pharmaceutical product. ( read more )..... Closed
06-0060 Pharmaceuticals consultant needed to provided Good Manufacturing Practices cGMP regulatory training ( read more )..... Closed
06-0057 Seasoned high level regulatory pharmaceuticals professional with expertise in parenterals, sustained release injectable dosage forms for development of NDA strategy and to assess : 1. Aseptic facili ( read more )..... Closed
06-0055 Clinical Pharmaceuticals Regulatory Consultant needed for clinical research training in the area of quality assurance / auditing techniques / auditor. ( read more )..... Closed
06-0039 Biotechnology company needs regulatory consultant to develop internal pharmacovigilance training materials ( read more )..... Closed
06-0037 Regulatory consultant needed to develop handbook for Training and Procedures for FDA Drug Safety Pharmacovigilance. ( read more )..... Closed
06-0036 GMP Pharmaceutical Regulatory Consultants needed to develop GMP training courses that are applicable to the countries outside of the US (Canadian and European regs mostly but Japan, etc. would be a bo ( read more )..... Closed
06-0031 Pharmaceuticals company needs recent ex-FDA Medical reviewer, now consultant, from the Division of Antiviral Drugs who can assist in clinical/regulatory strategy. ( read more )..... Closed
06-0028 Consultant needed to conduct marketing survey to assess potential in Brazil for finished pharmaceutical formulations from selected therapeutic categories. ( read more )..... Closed
06-0026 API manufacturer needs regulatory consultant to convert 2 European DMF's (in CTD format) for 2 of our API's (in English)into the required Japanese format for lodgement with our clients and the Japanes ( read more )..... Closed
06-0024 Pharmaceutical consultant or attorney needed for start-up OTC pharmaceutical manufacturer. Consulting includes registration, trademark, NDC and Bar Code Label applications, & other. ( read more )..... Closed
06-0023 FDA and ISO phramceuticals consultants to provide training on Validation and Qualification of computer systems in the pharmaceuticals industry with respect to FDA regulatory compliance. ( read more )..... Closed
06-0020 Former FDA consultant needed to conduct mock FDA inspection for European IVD manufacturer (product includes reagents, instrument & software) in preparation for first FDA inspection. ( read more )..... Closed
06-0018 Regulatory consultants needed for ANDA Application for generic pharmaceutical controlled release tablet formulations. ( read more )..... Closed
06-0016 Pharmaceutical Consultant needed for Pharmaceuticals Good Manufacturing Practices (GMP) training for Pharmaceutical labeling and packaging company. ( read more )..... Closed
06-0015 Pharmaceutical Consultants needed for on-site validation of automated pharmaceutical process equipment for manufacturer of pharmaceutical equipment ( read more )..... Closed
06-0014 API manufacturer needs USFDA Regulatory Consultant well versed with FDA regulations for approval of Active Pharmaceutical Ingredient (API) facility by USFDA Authorities in India. It is a green field ( read more )..... Closed
06-0009 "FDA, GMP Contract Sterilizer needed to sterilize oil that will be used for implantation drug use and heart stents. This needs to be done without harming the oil's effectiveness. " ( read more )..... Closed
06-0008 "FDA consultancy for set-up of pre-IND meeting. Advice on development programme & identification of suitable clinical experts. Therapeutic area is short acting sedatives/anasthesia." ( read more )..... Closed
06-0007 UK based biotech / pharmaceuticals company that is looking to file and IND and NDA applications in the US. We need a consultant who would be prepared to act as our US agent?" ( read more )..... Closed
06-0004 "On-Line or Direct training on FDA ,EMEA ,MCA guidelines for the registration of pharmacuticals as well as herbal products" ( read more )..... Closed
05-0064 Experienced Pharmaceutical Regulatory Consultant needed to assist RA Manager in reviewing content and assembling ANDA for submission in early January" ( read more )..... Closed
05-0063 Quality Consultant needed for SOP writing and compliance consulting. Need SOP put in place for GLP compliant bioanalytical testing" ( read more )..... Closed
05-0062 Experienced US FDA Biopharmaceutical Regulatory Consultant needed for foreign biopharmaceutical company entering US. Consultant will provide guidance for regulatory process required to get FDA approva ( read more )..... Closed
05-0059 EU consultant needed to advise on reimbursement issues in each of the 5 EU countries. We are interested in having a conversation with regulatory experts in the EU for a new pharmaceutical. There a ( read more )..... Closed
05-0056 "Pharmaceuticals manufacturer needs regulatory consulting firm to review and submit pharmaceuticals ANDA. We have prepared ANDA as per available format and like to be reviewed by an external adviser ( read more )..... Closed
05-0055 Pharmaceutical regulatory consultants needed to assemble EU dossiers for our products." ( read more )..... Closed
05-0054 Pharmaceutical regulatory consultants needed for converting old-style European DMFs into CTD (and eCTD) format. If you offer this service, please inform me of your rates and schedule availability. " ( read more )..... Closed
05-0049 Regulatory compliance consulting needed in Toronto for importing OTC products into Canada. Experience with DIN, NHP and HealthCanada is required. ( read more )..... Closed
05-0043 Pharmaceuticals Clinical Trials consultant needed to design a phase I clinical protocol to support an IND application for a fixed dose combination drug. Looking for consultant with experience worki ( read more )..... Closed
05-0042 Regulatory Consultant needed to consult and develop registration procedures and the Documents needed for filing dossiers of Pharmaceutical Products in all the following CIS countries: 1. Armenia ( read more )..... Closed
05-0037 Regulatory consultant needed for assistance and information regarding FDA's new "IDE Probability Sampling Survellance Inspections"? "" ( read more )..... Closed
05-0036 Consultants needed for patent for new generation Antaacid preparation is open for licencing.Compositions in our invention are not based primarily on alkali metal or alkaline earth metal compounds and ( read more )..... Closed
05-0027 Regulatory consultant needed for consulting on Homeopathic Drug, manufactured and registered in Germany. Need to know viability and process to import into the US and market as OTC Drug (poss. mail or ( read more )..... Closed
05-0026 Pharmaceutical Regulatory Consultant needed as a Liasoning Officer to get Medicinal formulation register in South East Asian countries. We are R&D organization , with company registered in Germany. We ( read more )..... Closed
05-0019 USFDA GMP pharmaceutical consultant knowledgeable of the regulatory (cGMP, FDA, contract manufacturing) requirements, guidelines for contract manufacturing of specifically, excipients needed . Experie ( read more )..... Closed
05-0017 USA FDA GMP sterile contract manufacturer needed for clinical supply manufacruting for IND to make intralipid like emulsified product for IV. Need US cGMP facility to make 10 L stable, sterile batch f ( read more )..... Closed
05-0015 Quality Consultants needed for in-house GLP, Quality,GMP and ISO training for company beginning to meet compliance. Looking for set-up (initial) basic training for GLP, Quality Systems , GMP, and ISO ( read more )..... Closed
05-0014 "Pharmaceutical Distribution Channel Expert. We are expecting to acquire some already approved pharmaceutical products. Current NDC holder has 8 months inventory in the channel. Don't want to wait to ( read more )..... Closed
05-0011 FDA GMP Pharmaceutical contract manufacturer needed to manufacturer Ergonovine Maleate 0.2mg tablets""" ( read more )..... Closed
05-0010 Medical Gas Company needs pharmaceutical regulatory consultants to assist with compliance issues ( read more )..... Closed
05-0008 "Manufacturing assistance and consulting needed to manufacture the following APIs: Ferrous Fumarate, Hydroxypropyl Methylcellulose, Sodium crosscarmellose" ( read more )..... Closed
05-0006 FDA Consultant needed for FDA PAI & GMP consulting and resources for foreign establishment" ( read more )..... Closed
05-0005 USA FDA GMP consultant neeeded for Pharmaceutical GMP Vendor Audit Checklist. Budget $99 " ( read more )..... Closed
05-0003 FDA GMP regulatory consultants to audit pharmaceutical manufacturing facility for cGMP compliance and other related services for pharmaceutical manufacturer." ( read more )..... Closed
05-0002 Pharamceutical Regulatory Consultants needed for pharmaceutical IND, CTA, CTD consulting assistance on Australian, European, Canadian and UK regulatory policies and procedures regarding INDs, CTAs and ( read more )..... Closed
05-0001 Former MHLW Reviewer Regulatory consultant fluent in Japanese needed to advice pharmaceutical company on regulatory matters in Japan. Specifically, former MHLW reviewer who now works as a regulatory c ( read more )..... Closed

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