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

Clinical Trials Regulatory Consulting Requests

Global Regulatory.com has received the following incoming Clinical Trials Consulting Requests which need to be fulfilled ! These Clinical Trials Consulting Requests are received from a variety of sources ranging from start-up companies to large, multinational corporations actively seeking consultants to perform their Clinical Trials 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 Clinical Trials Consulting Requests
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Clinical Trials consulting request description
status
13-0003 Need an independent License A holder regulatory resource to submit completed package for clinical trial approval ( read more ).....
This is a course that anyone in a hospital or clinic who might be involved in conducting a clinical trial should take. If they have never been involved they will learn what one is, if they have done c ( read more ).....
A 505(b)2) product is an improved or altered version or a new use application for a previously FDA-approved drug. This unique regulatory pathway, available only for marketing approval in the US, offer ( read more ).....
12-000015 Clinical Regulatory consultant needed to clarify regulatory requirements for clinical trials in Senegal. Services needed to create a comprehensive Country Regulatory Profile. ( read more ).....
12-000002 In-Vitro diagnostics IVD FDA Regulatory consultant to assist with clinical trials and 510(k) submissions for FDA Class I and II devices. ( read more ).....
11-000120 USA clinical trial sponsor needs information on importing into sites in the Dominican Republic. Specifically: 1) Do the sites need to obtain the import permit from the Ministry of Health or may a th ( read more )..... Closed
11-000061 This is a cost estimate only: We need a highly qualified auditor to provide costing to accomplish the following: Perform a Center-Initiated Regulatory Compliance Audit (specifically with respect t ( read more )..... Closed
11-000031 China independent consultant needed with a deep understanding of the SFDA (& FDA) regulatory environment and requirements;local experience in regulatory applications for clinical trials and registrati ( 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
10-00064 Regulatory Consultant needed for regulatory advice / local document review / submission support for an observational, non-drug trial to be conducted by one of our Sponsors ( read more )..... Closed
10-00062 Regulatory Consultant needed to submit protocol in Hungary, Spain, Italy and Austria. We will be able to supply the application for Belgium and France. We do not need the same person to be able to d ( 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
09-0176 Clinical Trial Regulatory COnsultat with expertise in Colombia who can provide guidance on what is required for submission (IND equivalent) to INVIMA for conduct of a clinical study. ( 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
09-0119 Regulatory consultant needed in Italy to obtain Italian Azienda di Sanita Locales (ASLs)approvals in the regions of Lombardia, Piedmonte, and Emilia-Romagna so that we can expand our healthcare screen ( read more )..... Closed
09-0109 Require help with filling in the METC ABR form for the Dutch regulatory authorities with view to making application for clinical trials in Netherlands. ( 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
09-0080 Pharmaceutical Mfg needs qualified ANVISA consultant to audit CRO for BE/BA studies for ANVISA (Brazil) ( read more )..... Closed
09-0071 Biologics Company needs Clinical Trial, Toxicology COnsulting Group to design stem cells trials, cord, placental, autologous cells, human trials for toxicity. Effects of above on chronic disease ( read more )..... Closed
09-0025 Clinical Trail Regulatory Consultant needed to advise on MOH Submissions and regulatory process in Belize. For example, how does the MOH submission take place and then does an IRB approve the study? ( read more )..... Closed
09-0019 India based CRO,looking to conduct Clinical trials/ BA/BE studies/ Phase I studies for companies of the Gulf. We have been told that we require a "GULF CORPORATE COUNCIL CERTICATE" for this. Our compa ( read more )..... Closed
09-0006 Medical Device Regulatory Expert in Brazil familiar with ANVISA registration process needed to assist and to provide information about the clinical trials that are required for Class I medical devices ( read more )..... Closed
08-0164 Qualified GCP auditor needed to audit a Phase 3 clinical studies ( read more )..... Closed
08-0161 Clinical Trial Consultant needed to assist in providing information on Institutional Review Board rules and regulations ( read more )..... Closed
08-0152 Clinical Trials Consultant needed for grant writing for a SBIR grant for an innovative Clinical Trials application implemented as Software as a Service. I am looking for a consultant to spend 80-100 ( read more )..... Closed
08-0139 Regulatory Auditor needed to conduct mock FDA style audit and gap analysis of contract laboratory in India that is conducting clinical testing for health care personnel hand wash products. ( 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
08-0119 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
08-0083 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
08-0040 Quality Systems consultant needed for quality system development in clinical trials and pharmacovigilance. ( read more )..... Closed
08-0032 We are a high complexity molecular diagnostics lab with CLIA and CAP certification with licenses in TN, NY, VA, FL. ALso are performing increasing amount of clinical trials work for variety of pharma, ( read more )..... Closed
07-0148 An exciting opportunity at a major Global Pharmaceutical organisation based near Brussels. Interim consultant needed to assist with Clinical Trial Applications to EU and International markets. ( read more )..... Closed
07-0135 Pharmaceutical clinical trial consultant needed for developing FDA GCP clinical trial for new drug rimonabant ( read more )..... Closed
07-0124 CLinical Trials consultants needed to advise on regulatory requirements needed for implementing studies in Mexico. ( read more )..... Closed
07-0064 Clinical Trial COnsultant needed for setting up Pharmaceutical Clinical Trials in Romania. ( read more )..... Closed
07-0014 Clinical Consultant needed for clinical trials training in pharmaceuticals,medical devices,cosmetics,food and beverages ( read more )..... Closed
06-0157 Need information regarding setting up clinical trials in Romania. ( read more )..... Closed
06-0099 Clinical Trial Consultant needed for consulting on phase I, II, III and IV clinical trials in Cyprus, Israel, Botswana, Bahamas, Luxembourg, El Salvador, Jamaica, New Zealand, Turkey, Uruguay and Bulg ( 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
06-0089 Clinical Consultant needed to advise on standards for immunological clinical trials for blood collection in paediatric populations after vaccination for immuno assay. Advising on standards in India. ( read more )..... Closed
06-0017 Regulatory consultant needed to develop GLP Phase I studies for a USFDA Investigational New Drug IND Application for a nutraceutical. ( read more )..... Closed
05-0061 Regulatory clinical trials consultant needed for consulting on guidelines and approvals to conduct a clinical study for natural nutraceuticals ( read more )..... Closed
05-0057 ""Large Medical Device Company seeking a service provider for the selection, establishment, and management of a DSMB for a cardiovascular medical device clinical trials study."" ( read more )..... Closed
05-0053 Contract Research Organization needed for evaluation of a food supplement for needs for toxicology studies and human efficacy. "" ( read more )..... Closed
05-0051 ""on-site 3-5 day training session for clinical trials/monitoring for auditors. 10-15 persons for the first week of December 2005"" ( read more )..... Closed
05-0044 Clinical Trials Consultant needed to consult on Regulatory requirements for clinical study submissions for both Ethiopia and Gambia"" ( 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
05-0041 International regulatory consulting group needed to assist virtual pharmaceutical company with regulatory strategy for conduct of clinical trials in the EU, and ultimate registration of products in th ( read more )..... Closed
05-0040 Regulatory consultant needed in submitting Clinical Trial Application in Canada for Drug trial underway in USA""" ( read more )..... Closed
05-0028 CLIA certified lab needs CLIA consultant for consulting on CLIA compliance. We want to make sure our lab is prepared in the event that we are the recipients of an official inspection. """ ( 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

For more information on Clinical Trials consulting services, please call 1-403-770-1994 or email Global Regulatory

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