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Directive 2001 83 EC
Results: 312

#	Item
201	PUBLIC CONSULTATION PAPER ON THE REGULATION ON ADVANCED THERAPY MEDICINAL PRODUCTS 2.1. Marketing authorisation application requirements for advanced therapy medicinal products. The Advanced Therapy Regulation provided f Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:28 Research Pharmaceuticals policy Pharmaceutical industry Pharmacy Pharmacology European Medicines Agency Medical device Cell therapy Directive 2001/83/EC Clinical research Pharmaceutical sciences Medicine
202	EBE Comments on PUBLIC CONSULTATION PAPER ON THE REGULATION ON ADVANCED THERAPY MEDICINAL The paper identifies 5 consultation topics. 1. Marketing authorisation application requirements for advanced therapy medicinal pro Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 Medicine Pharmaceuticals policy Pharmaceutical industry European Union Cell therapy Medical device Validation Food and Drug Administration Directive 2001/83/EC Clinical research Research Biology
203	Co-ACT response to the European Commission’s invitation to submit comments as part of the public consultation on Regulation[removed] (“ATMP Regulation”) Co-ACT welcomes the initiative of the European Commission an Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 Research Science Pharmaceuticals policy Pharmaceutical industry Pharmacy Clinical trial Directive 2001/83/EC Clinical research Pharmaceutical sciences Pharmacology
204	Public Consultation on the Regulation of ATMPs Pfizer Feedback REGULATION ON ADVANCED THERAPY MEDICINAL PRODUCTS Pfizer Feedback to the European Commission on the Public Consultation Paper INTRODUCTION Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:34 Pharmaceutical sciences Pharmacology Pharmaceuticals policy Pharmaceutical industry European Medicines Agency Medical device Pfizer Traceability Directive 2001/83/EC Clinical research Research Medicine
205	Permettre l’examen simplifié des modifications Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:35:13 Clinical research Health Pharmacy Drug safety European Medicines Agency Pharmacovigilance EudraPharm Directive 2001/83/EC Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy Pharmacology
206	Headquarters Executive Office Gyle Square 1 South Gyle Crescent EDINBURGH EH12 9EB Telephone[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:41 Stem cells Pharmaceuticals policy Cell biology European Medicines Agency Cell therapy EudraLex European Directorate for the Quality of Medicines Directive 2001/83/EC Embryonic stem cell Biology Clinical research Biotechnology
207	CMDh QUESTIONS & ANSWERS PRODUCT INFORMATION / INFORMATION ON MEDICINAL PRODUCTS Doc. Ref.: CMDh[removed], Rev0 October 2012 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-08-08 03:51:36 Health policy Health EudraLex Directive 2001/83/EC Pharmaceuticals policy Clinical research Research
208	CMDh QUESTIONS & ANSWERS HOMEOPATHIC MEDICINAL PRODUCTS Doc. Ref.: CMDh[removed], Rev0 October[removed]HOMEOPATHIC MEDICINAL PRODUCTS DISAGREEMENT IN PROCEDURES REFERRAL Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-12-19 08:45:43 Pseudoscience Pharmaceuticals policy Research Pharmaceutical industry Homeopathy European Medicines Agency Directive 2001/83/EC Alternative medicine Regulation and prevalence of homeopathy Medicine Clinical research Health
209	Q&A TRADITIONAL HERBAL MEDICINAL PRODUCTS Doc. Ref.: CMDh[removed]Rev.01 JanuaryFebruary 2013 Question 1 What is the meaning of a “Community monograph” in the context of MRP/DCP of traditional Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-03-07 04:51:58 Research Pharmaceuticals policy Pharmaceutical industry European Union European Medicines Agency Herbalism Herbal Directive 2001/83/EC Alternative medicine Clinical research Medicine Health
210	83 Borderline Working Group Regulatory Framework, Jurisprudence (case-law) and Guidance Documents Add to Reading List Source URL: www.hma.eu Language: English - Date: 2012-12-19 12:31:10 Law European Union European Union law Directive 2001/83/EC Biocidal Products Directive European labour law Directive 93/41/EEC Pharmaceuticals policy European Union directives Clinical research

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