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Directive 2001 83 EC
Results: 312

#	Item
241	Comments on the Concept Paper on DELEGATED ACT ON THE DETAILED RULES FOR A UNIQUE IDENTIFIER FOR MEDICINAL PRODUCTS FOR HUMAN USE, Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:10 Directive 2001/83/EC Pharmaceuticals policy Clinical research European Union
242	Delegated Act on the Detailed Rules for a Unique Identifier for Medicinal Products for Human Use, and its Verification Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:40:50 Identifiers Business Electronic commerce Barcodes Radio-frequency identification Wireless Packaging and labeling Directive 2001/83/EC GS1 Technology Identification Automatic identification and data capture
243	EGA COMMENTS ON THE CONCEPT PAPER ON THE DELEGATED ACT FOR A UNIQUE IDENTIFIER FOR MEDICINAL PRODUCTS FOR HUMAN USE, AND ITS VERIFICATION. EGA’S COMMENTS ON THE CONCEPT PAPER SUBMITTED FOR PUBLIC Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:10 Pharmacology Pharmacy Clinical research Drug safety Directive 2001/83/EC Pharmacovigilance Online pharmacy Pharmaceutical industry Pharmaceutical sciences Health Pharmaceuticals policy
244	ega-pos-pap[removed]ec-consultation-counterfeit medicines &慭瀻 api gmp-FINAL Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2011-09-02 06:31:46 Pharmacology Health Pharmacy Clinical research Good manufacturing practice Good distribution practice Counterfeit medications Traceability Directive 2001/83/EC Pharmaceuticals policy Pharmaceutical sciences Pharmaceutical industry
245	REASONED OPINION On the Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL, on fees payable to the European Medicines Agency for the conduct of pharmacovigilance activities in respect of medicinal pr Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-09-27 11:02:20 Health Pharmacology Drug safety Pharmacy European Medicines Agency Pharmacovigilance Directive 2001/83/EC Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance Pharmaceutical sciences Clinical research Pharmaceuticals policy
246	Proposal for revision of guideline_Track changes March 2012 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:02:33 Pharmaceutical sciences Biology Pharmaceutical industry European Medicines Agency European Union Alternative medicine Directive 2001/83/EC Cell therapy EudraLex Clinical research Research Pharmaceuticals policy
247	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – quality, safety and efficacy Implementation Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-03-28 08:54:56 European Union directives Law European Union Directive 2001/83/EC EudraLex Government Framework decision European labour law Pharmaceuticals policy Clinical research European Union law
248	Internal Market and Service DG - Legislation in force - State of play as of[removed]Type N° Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-01-24 04:38:37 Pharmaceuticals policy Evaluation Reference European Union Standards Directive 2001/83/EC Clinical Trials Directive Markets in Financial Instruments Directive Computer Programs Directive European Union directives Law Clinical research
249	Biennial Report under Article 21 of Regulation (EC) No[removed]Introduction With regard to the application of Regulation (EC) No[removed], Bulgaria adopted Regulations on the conditions and procedures for involveme Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2012-03-13 12:02:40 Law Consumer protection law Directive 2001/83/EC Consumer protection Directive 75/319/EEC Clinical Trials Directive Pharmaceuticals policy Clinical research European Union
250	Microsoft Word - Variations-Co-decision Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:07:05 Directive 2001/83/EC Directive Directive 75/319/EEC Law Directive 75/318/EEC Pharmaceuticals policy Clinical research European Union

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