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09 September 2010

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Registrations, Submissions, Filings and Licenses Consulting Requests

Global Regulatory.com has received the following incoming Registrations, Submissions, Filings and Licenses Consulting Requests which need to be fulfilled ! These Registrations, Submissions, Filings and Licenses Consulting Requests are received from a variety of sources ranging from start-up companies to large, multinational corporations actively seeking consultants to perform their Registrations, Submissions, Filings and Licenses 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 Registrations, Submissions, Filings and Licenses Consulting Requests
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Registrations, Submissions, Filings and Licenses consulting request description
status
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 ).....
10-00120 Regulatory Company needed for EC, AEMPS submissions for approval of clinical study approximately 3 sites in Spain ( read more ).....
10-00119 EU, Canada and USA cosmetic labeling requirements. ( read more ).....
10-00117 CRO needs regulatory consultant for Anvisa approval of facility. ( read more ).....
10-00116 Regulatory Compnay needed to help obtain proper licence's in China, Japan, Mexico and more country's as we grow. ( read more ).....
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 ).....
10-00113 Pharmaceutical Manufacturer needs regulatory consultant to advise on registration of pharmaceuticals in Hong Kong ( read more ).....
10-00110 Netherlands CE certified Medical device & consumable company (ophthalmic products) needs regulatory consultant for registration in Latin American countries, especially Mexico and Argentina. All our p ( read more ).....
10-00104 Regulatory Consultant needed to assist in registering Ethical and OTC drug in Australia. ( read more ).....
10-000102 Thailand Pharma Company needs regulatory consultant for HIV drug registration ( read more ).....
10-00100 Singapore based company with R&D facility in Australia needs consultant to assist with requirement for having collogen cream imported and sold in China. ( read more ).....
10-00099 Medical Device Manufacturer needs Regulatory Consultant to Register contact lens products in UAE ( read more ).....
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 ).....
10-00094 Israel company needs regulatory consultant for Regulatory compliance and Filings for import of Hand Sanitizer to HK and China. ( read more ).....
10-00092 US Cosmetics Company looking for consulting help to distribute finished good cosmetic products in Europe, South America (Mexico and Brazil) and Japan ( read more ).....
10-00091 Beverage Manufacturer needs Food Regulatory Consultant for Country by country approval for importation and distribution of beverage products ( read more ).....
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 ).....
10-00086 Israel Cosmetics Company needs consultant expert in registering "Cosmetics with a Claim" with the Israeli Ministry of Health. ( read more ).....
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 ).....
10-00083 Brazil Regulatory Expert needed for Registration of products in Brazil: instruments and reagents. ( read more ).....
10-00082 Pharmaceutical Regulatory expert needed for NDA and drug monograph submissions for a natural product. ( read more ).....
10-00074 part time regulatory consultant in Japan needed to oversee building of lab as well as submission of about 18 skus to the Ministry of Health. This person should be bilingual and have worked with cosm ( read more )..... Closed
10-00073 USA based company seeking regulatory consultant who can help us to register our rapid ivd screening devices in Mexico's "FDA" equivalent (COFEPRIS?). ( read more )..... Closed
10-00072 NY Company has product registered with US EPA and needs Canada Consultant to register it with Canada PRMA. ( read more ).....
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
10-00070 Turkish representative needed to register our products (resins)that we export to Turkey. Upcoming new legislation requires us to do so. ( read more )..... Closed
10-00069 Medical Device Manufacturer needs FDA Regulatory Consultant for 510K approval Classification Panel: Radiology Diagnostic Devices Classification name: Positron Camera, Class I, 21 CFR § 892.1110 Pr ( read more )..... Closed

For more information on Registrations, Submissions, Filings and Licenses consulting services, please call 1-403-770-1994 or email Global Regulatory

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