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Medical Products Agency
Results: 228

#	Item
191	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, EMA PHARM 628 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-30 04:33:16 Health Pharmaceutical sciences European Medicines Agency Directive 2001/83/EC Medical device Medicinal product Medical Devices Directive Supplementary protection certificate European Directive on Traditional Herbal Medicinal Products Pharmaceuticals policy Clinical research Medicine
192	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products e-Health and Health Technology Assessment Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-05-27 09:38:34 Prediction Time European Network for Health Technology Assessment Medical technology Health technology assessment Technology assessment Agency of the European Union HTML Application European Union Evaluation Impact assessment Technology
193	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency PHARM 616 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:48:14 Health Clinical research Pharmaceutical industry Pharmaceuticals policy Pharmacy European Medicines Agency Pharmacovigilance Medical device Alternative medicine Medicine Pharmaceutical sciences Pharmacology
194	COMMITTEE ON THE SAFETY OF DEVICES 7 November 2013 MHRA, 151 Buckingham Palace Road, London, SW1W 9SZ CSD Dr Sheila Fisher (Chair) Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-01-20 12:08:50 Medical equipment Medical device Medical technology Breast implant National Institutes of Health National Health Service Medicines and Healthcare products Regulatory Agency Medicine Health Department of Health
195	UK regulation of Blood Safety & Quality, [removed] Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2012-03-13 14:13:52 Pharmaceutical industry Transfusion medicine Medical terms Hematology Medicines and Healthcare products Regulatory Agency Yellow Card Scheme Adverse effect Patient safety Adverse event Medicine Health Clinical research
196	Notes for applicants and holders of a Manufacturer’s Licence MHRA Guidance Note 5 1 Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-03 12:41:08 Pharmaceutical industry Clinical research Health Good manufacturing practice European Directive on Traditional Herbal Medicinal Products Qualified Person European Medicines Agency Medical device EudraLex Pharmaceuticals policy Medicine Pharmaceutical sciences
197	MHRA Business Plan[removed] Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2012-05-04 12:03:07 Pharmaceutical industry Clinical research Pharmacology Clinical trial Design of experiments Drug discovery Medical device Medicines and Healthcare products Regulatory Agency European Medicines Agency Medicine Pharmaceutical sciences Health
198	Microsoft Word - A Guide to Defective Medicinal Products_FINAL.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-03-05 09:44:00 Pharmaceutical industry Pharmaceuticals policy Pharmacy Medical device Medical equipment Good manufacturing practice Product recall Medicines and Healthcare products Regulatory Agency Pharmaceutical sciences Medicine Pharmacology
199	Corporate Plan[removed] Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-04-11 11:41:47 Clinical research Pharmaceutical industry Pharmacology Pharmacy Department of Health Medicines and Healthcare products Regulatory Agency Pharmacovigilance Medical device Good Laboratory Practice Medicine Health Pharmaceutical sciences
200	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