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Medical Products Agency
Results: 228

#	Item
201	Serious Adverse Blood Reactions and Events (SABRE) User guide for mandatory haemovigilance reporting in the UK Published by the MHRA, the UK competent authority for Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2012-02-07 07:22:52 Transfusion medicine Pharmaceutical industry Patient safety Hematology Medicines and Healthcare products Regulatory Agency Adverse effect Medical device Blood donation Blood transfusion Medicine Health Clinical research
202	MEDICINES AND HEALTHCARE PRODUCTS REGULATORY AGENCY Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-01-24 06:53:01 Clinical research Pharmaceutical industry Department of Health Pharmacy Pharmacology European Medicines Agency Medicines and Healthcare products Regulatory Agency Medical device Pharmacovigilance Pharmaceutical sciences Medicine Health
203	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
204	PUBLIC CONSULTATION PAPER ON THE REGULATION ON ADVACED THERAPY MEDICINAL PRODUCTS Comments by Dr. Martin Fussenegger MD Head surgeon of ENT Dept. Klinikum Wels-Grieskirchen Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:37 Fertility Fertility medicine In vitro fertilisation Pregnancy Reproduction Medical device European Medicines Agency Medicine Biology Cryobiology
205	Borderline Working Group Borderline Network Contact Points for Classification of Veterinary Medicinal Products Version dd. 1 April[removed]September 2012 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2014-04-03 10:44:17 Executive agencies of the United Kingdom government Veterinary Medicines Directorate Danish Medicines Agency Biocide Medical device Veterinary physician European Medicines Agency Medicine Health Pharmaceutical sciences
206	Microsoft Word - ACS V9 06 Mar 12.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2012-05-02 09:49:59 Health Pharmaceutical sciences Clinical research Department of Health Medicines and Healthcare products Regulatory Agency Yellow Card Scheme Medical device Good manufacturing practice Medicine Pharmaceutical industry Pharmaceuticals policy
207	Guidance for mfrs on clinical trials Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-11-01 11:48:10 Clinical research Health Medical technology Validity Medical equipment Medical device Medicines and Healthcare products Regulatory Agency CE mark Food and Drug Administration Medicine Pharmaceutical industry Technology
208	Regulation and Accreditation Proposal (RAMS) Sectorial Market Surveillance Programme for Medical Devices Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-06-24 07:24:31 Pharmaceutical industry Consumer protection law Health Medical equipment Department of Health Medicines and Healthcare products Regulatory Agency Medical device Medical Devices Directive CE mark Medicine Clinical research Technology
209	Corporate Plan[removed] Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-08-28 07:44:52 Pharmaceutical industry Clinical research Pharmacology Pharmacy Drug safety Medicines and Healthcare products Regulatory Agency Medical device Pharmacovigilance National Health Service Medicine Pharmaceutical sciences Health
210	Requirements for notified bodies Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-11-01 11:20:25 Medical equipment Medical technology Product certification Clinical research Pharmaceutical industry CE mark Notified Body Medical device Medicines and Healthcare products Regulatory Agency Medicine Technology Health