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Qualified person
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401	Vienna, 27 March[removed]SANCO/D/6/SF/mg/ddg1.d[removed]PHARMIG response to the European Commission Draft: Template for the Qualified Person’s Declaration Concerning GMP Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:26 Audit Qualified Person Auditing Pharmaceuticals policy Information technology audit Clinical research
402	Microsoft Word - QPAssociation_CounterfeitMedSurvey_CoverLetter.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:03:03 Counterfeit consumer goods Clinical research Council of Europe European Directorate for the Quality of Medicines Counterfeit medications Qualified Person Good distribution practice Pharmaceuticals policy Pharmaceutical industry Health
403	Microsoft Word - QPAssociation_CounterfeitMedSurvey_Comments.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:03:05 Pharmacology Health Clinical research Vetter Pharma Food and Drug Administration Qualified Person Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme Quality management system Counterfeit medications Pharmaceutical industry Pharmaceutical sciences Pharmaceuticals policy
404	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
405	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:37 European Medicines Agency Qualified Person Pharmaceutical sciences Pharmacology Clinical research Research Pharmaceutical industry
406	Microsoft Word - QPAssociation_Comment_Draft EU GDP Guide.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:38 Quality Validation Validity Qualified Person Good distribution practice Systems engineering process Science Evaluation Form Pharmaceuticals policy Pharmaceutical industry Clinical research
407	Form for submission of comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:42 Pharmaceutical sciences Pharmaceuticals policy Pharmaceutics European Medicines Agency Validation Qualified Person Clinical research Pharmaceutical industry Research
408	GE Healthcare: Commission Guidelines on Good Distribution Practice of Medicinal Products for Human Use GE Healthcare Commission Guidelines on Good Distribution Practice of Medicinal Products for Human Use Date: 20 Decem Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:43 Quality Business Technology Science Good distribution practice Validation Qualified Person Packaging and labeling Alternative medicine Pharmaceuticals policy Clinical research Pharmaceutical industry
409	Ref. Ares[removed][removed]Rue de la Loi 26, Box[removed]Brussels, Belgium the vital unk in healthcare GROUPEMENT INTERNATIONAL DE LA RÉPARTITION PHARMACEUTIQUE - EUROPEAN ASSOCIATION OF PHARMACEUTICAL FULL-LI Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:37:44 Clinical research Pharmaceutics Pharmacology Quality Good distribution practice Good manufacturing practice Validation European Medicines Agency Qualified Person Pharmaceutical industry Pharmaceuticals policy Pharmaceutical sciences
410	Brussels, xx December 2009 F2/2009/D/2102 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 08:56:16 Hematology Pharmaceuticals policy Biology Transfusion medicine Pharmaceutical industry EudraLex Plasmapheresis Blood bank Qualified Person Medicine Clinical research Anatomy

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