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Qualified person
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#	Item
331	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Add to Reading List Source URL: www.nmvrvi.lt Language: English - Date: 2012-12-13 15:43:53 Pharmacology Health Drug safety Pharmacy European Medicines Agency Qualified Person for Pharmacovigilance Drug Master File Marketing authorization Test data exclusivity Pharmaceutical sciences Pharmaceutical industry Pharmaceuticals policy
332	From: MPT - Ian McCorquodale[SMTP:[removed]] Sent: Wednesday, January 15, [removed]:08:47 AM To: ADM-GMDP Subject: Concerns regarding draft Annex16 of Volume 4 of EU Guidelines for Good Manufacturing Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-01-31 06:07:24 Pharmaceuticals policy Clinical research Qualified Person
333	DELEGATED ACT ON THE PRINCIPLES AND GUIDELINES OF GMP FOR ACTIVE SUBSTANCES IN MEDICINAL PRODUCTS FOR HUMAN USE Response of the Czech Republic to the Concept Paper submitted for public consultation 1. Extension of the Di Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:53 Qualified Person EudraLex Directive Health Science Pharmaceuticals policy Clinical research Medicinal product
334	Revision July[removed]Application Form for Renewal of a Marketing Authorisation Add to Reading List Source URL: nmvrvi.lt Language: English - Date: 2013-08-14 07:16:53 Pharmacology Health Drug safety Pharmacy Qualified Person Pharmacovigilance Supplementary protection certificate European Medicines Agency Pharmaceutical sciences Pharmaceuticals policy Clinical research
335	COUNCIL OF THE EUROPEAN UNION Brussels, 25 June[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:10 Pharmaceuticals policy Health Medicine Drug safety Pharmacy Pharmacovigilance Medicinal product European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Clinical research Pharmacology
336	EIPG COMMENTS on Sanco.ddg1.d[removed]Extension of the Directive on GMP for medicinal products to active substances Consultation Item No 1: Do you agree with this appraisal and approach? Yes, we agree with this app Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:44:17 EudraLex Medicinal product Qualified Person Law Government Clinical Trials Directive Directive 2001/83/EC Pharmaceuticals policy Clinical research Health
337	Comments on the Concept Paper submitted for Public Consultation concerning the Delegated Act on Principles and Guidelines of Good Manufacturing Practice for Active Substances in Medicinal Products for Human use. Ref: San Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:49 Pharmaceutical sciences Health policy EudraLex Good manufacturing practice Qualified Person Medicinal product Directive 2001/83/EC Validation Qualified Person for Pharmacovigilance Pharmaceuticals policy Clinical research Research
338	COUNCIL OF THE EUROPEAN UNION Brussels, 22 September[removed]OR. en[removed] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:08 Research Health European Medicines Agency Pharmacovigilance Supplementary protection certificate Qualified Person Responsible For Pharmacovigilance Clinical research Pharmaceuticals policy Pharmaceutical sciences
339	Portrait of a cheerful boy with loving parents and grandparents Add to Reading List Source URL: www.egagenerics.com Language: English Health Pharmacovigilance Adverse effect Pharmaceutical industry Pharmaceutical drug Qualified Person Responsible For Pharmacovigilance European Medicines Agency Pharmacology Pharmaceutical sciences Medicine
340	MULTI-JURISDICTIONAL GUIDE[removed]LIFE SCIENCES Italy Alberto Mocchi, Francesco Setti, Francesca Libanori and Add to Reading List Source URL: www.franzosi.com Language: English - Date: 2012-05-16 12:55:09 Pharmacology Health Drug safety Intellectual property law Supplementary protection certificate European Medicines Agency Qualified Person Responsible For Pharmacovigilance Summary of Product Characteristics Pharmacovigilance Pharmaceuticals policy Pharmaceutical sciences Clinical research

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