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Archemin offers various services in the European Community: - Regulatory Strategy review - New applications - Post approval procedures - pricing and reimbursement - Dossier updates - Line extensions - Variations - Licence renewals - Pharmacovigilance services - Medical Information
PIL readability testing performed in Dutch, French and English
Archemin has extensive experience in medical and technical writing: - Clinical and Non-clinical overviews and summaries - Pharmaceutical expert reports - SmPC - Periodic Safety Update Reports - Ecotoxicology assessments
Areas covered: Domestic Markets, Export Drugs, Clinical Trial Medication, Controlled Substances, Medical Devices ….
Last update of this entry: December 13, 2016
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