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Medical Products Agency
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#	Item
1	Quasi Drug Rules in Japan December 2011 Quasi-drugs are a unique product classification in Japan. A quasi-drug is defined in Japan as products that have minimal to moderate pharmacologic activity but are restricted in us Add to Reading List Source URL: www.jetro.go.jp Language: English - Date: 2015-03-30 22:38:04 Pharmaceuticals policy Health Pharmaceutical sciences Pharmaceutical industry Drugs Marketing authorization Pharmaceutical industry in China Over-the-counter drug Pharmaceuticals and Medical Devices Agency Cosmetics Pharmaceutical drug Food and Drug Administration
2	PSUR Submissions in Single Assessment via EMA Gateway Webclient An agency of the European Union Presenters of the Day, from EMA Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:50 Medical research Clinical data management Clinical research Health Pharmaceutical industry Health informatics Electronic common technical document Pharmaceuticals policy Marketing authorization Committee for Medicinal Products for Human Use Validation
3	The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes:  Medicinal Products Act (Official Gazette Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2013-07-12 06:13:47 Pharmaceuticals policy Health Medical research Clinical Trials Directive Directive 2001/83/EC Good laboratory practice Marketing authorization Good Clinical Practice Directive European Pharmacopoeia Biopharmaceutical Pharmacovigilance European Medicines Agency
4	COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 10 December 2008 SECVolume I Add to Reading List Source URL: www.myereport.eu Language: English - Date: 2015-11-08 06:14:30 Pharmaceuticals policy Health Medical research Pharmacovigilance European Medicines Agency EudraLex European Directive on Traditional Herbal Medicinal Products Postmarketing surveillance Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance
5	HMA/EMA Task Force on adherence to time tables Christer Backman, MPA 82th HMA MEETING Luxembourg Presidency of the Council of the EU 2015 Dubrovnik, 22-23 October 2015 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-11-27 10:53:15 Medical Products Agency Pharmaceutical industry
6	White Paper Proposal for a New Zealand Regulatory Scheme for Medical Devices Add to Reading List Source URL: mtanz.org.nz Language: English - Date: 2015-03-30 19:38:15 Medicine Medical equipment Medical technology Health Technology ISO 13485 Notified Body Global Harmonization Task Force CE marking Medical device Medsafe Medicines and Healthcare products Regulatory Agency
7	House of Commons Committee of Public Accounts Access to clinical trial information and the stockpiling of Tamiflu Add to Reading List Source URL: www.publications.parliament.uk Language: English - Date: 2014-01-02 11:39:46 Health Medical research Clinical research Healthcare quality Clinical pharmacology Pharmaceutical industry Oseltamivir Medicines and Healthcare products Regulatory Agency Influenza pandemic AllTrials Clinical trials registry Clinical trial
8	Affiliated to the Royal College of Pathologists The Steering Group includes members representing the following professional bodies: British Blood Transfusion Society Royal College of Obstetricians and Gynaecologists Add to Reading List Source URL: www.shotuk.org Language: English - Date: 2016-01-13 06:42:19 Transfusion medicine Hematology Blood Medical terminology Blood transfusion Transfusion reactions Patient safety Shot Medicines and Healthcare products Regulatory Agency Transfusion-related acute lung injury Adverse effect Transfusion
9	HMA PROCEDURES AND GOVERNANCE Status: VersionRevision: JulyClicking the Table of Contents and Section Titles navigates the document. Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-07-08 03:16:24 Agencies of the European Union Heads of Medicines Agencies Medical Products Agency Upper memory area European Medicines Agency HMA
10	Microsoft Word - Enf Strategy Finaldoc Add to Reading List Source URL: www.communityequipment.org.uk Language: English - Date: 2013-08-14 04:27:52 Clinical research Pharmaceutical sciences Department of Health Medicines and Healthcare products Regulatory Agency Pharmaceuticals policy European Directive on Traditional Herbal Medicinal Products Medical device Good Laboratory Practice Regulation of therapeutic goods Medicine Pharmaceutical industry Health