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321	DOC Document Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-04-07 03:45:24 Clinical research Pharmacology Actuarial science Drug safety Risk management Pharmacovigilance Clinical trial Safety EudraVigilance Ethics Management Risk
322	Commission on Human Medicines Annual Report 2010 Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-18 05:27:13 Clinical research Pharmaceutical industry Drug safety Pharmacy Medicines and Healthcare products Regulatory Agency Commission on Human Medicines British Pharmacopoeia Pharmacovigilance Adverse effect Pharmaceutical sciences Health Pharmacology
323	PDF Document Add to Reading List Source URL: www.mhra.gov.uk - Date: 2013-07-02 05:05:36
324	Microsoft Word - EL (14)A 11 Final Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-22 06:50:04 GlaxoSmithKline Enantiopure drugs Amoxicillin Phenols Matter Wockhardt Sodium Chemistry Pharmacology Beta-lactam antibiotics
325	Name of Recipient F11 to next Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-06-24 07:23:42 Pharmaceutical sciences Pharmaceutical industry Clinical research Medical device Medical equipment Medical technology Medicinal product European Medicines Agency Electronic cigarette Medicine Pharmacology Technology
326	Microsoft Word - Final web minutes CHM 19 June 2014.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-25 12:01:16 Clinical research Pharmaceutical industry National Health Service Pharmaceuticals policy Yellow Card Scheme Methadone European Medicines Agency Pharmacovigilance Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
327	Microsoft Word - CorpPlanFINAL120407.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2008-08-25 04:19:55 Clinical research Pharmaceutical industry Pharmacology Executive agencies of the United Kingdom government Department of Health Medicines and Healthcare products Regulatory Agency Pharmacovigilance Medical device Postmarketing surveillance Medicine Health Pharmaceutical sciences
328	THE REVISION OF EUROPEAN LEGISLATION ON MEDICAL DEVICES Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-04-04 12:09:53 Clinical research Pharmaceutical industry Medical technology Pharmaceuticals policy Medicines and Healthcare products Regulatory Agency Medical device Breast implant CE mark Regulatory requirement Medicine Health Medical equipment
329	Government response to the UK Early Access to Medicines Scheme consultation – March[removed] What is the Early Access to Medicines scheme? Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-03-14 06:21:13 Pharmacy Pharmaceutical industry Drug safety National Health Service National Institute for Health and Clinical Excellence Pharmacovigilance Alternative medicine Commission on Human Medicines Medicines and Healthcare products Regulatory Agency Pharmaceutical sciences Pharmacology Health
330	DOC Document Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-04-07 03:44:16 Health Research Pharmaceutical sciences Pharmacology Drug safety Public key certificate CE mark Good manufacturing practice EudraCT Pharmaceuticals policy Clinical research Pharmaceutical industry

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