Qualified person - PDFSEARCH.IO - Document Search Engine

Qualified person
Results: 450

#	Item
391	Setting the scene: new European Union Pharmacovigilance legislation November 2012 Presented by: Dr Peter Arlett Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:39:07 Health Pharmacy Clinical research Pharmaceuticals policy Pharmacovigilance European Medicines Agency Adverse drug reaction EudraVigilance Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Drug safety
392	Association Européenne des Spécialités Pharmaceutiques Grand Public Association of the European Self-Medication Industry Europäischer Verband der Arzneimittel-Hersteller AESGP comments on the Template for the Qualifi Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:25 Pharmaceuticals policy Quality assurance Audit Qualified Person Health Science Learning Clinical research Clinical Data Management EudraCT
393	7th May[removed]Contribution from Groupement des Pharmaciens de L’Industrie en Europe (European Industrial Pharmacists’ Group), to the Public Consultation in Preparation of a legal proposal to combat Counterfeit Medici Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:46:45 Pharmaceutical industry Research Health EudraLex Good distribution practice Directive 2001/83/EC Qualified Person Medicinal product Good manufacturing practice Pharmaceuticals policy Clinical research Pharmaceutical sciences
394	Submission of comments on TEMPLATE FOR THE QUALIFIED PERSON’S DECLARATION CONCERNING GMP COMPLIANCE OF INVESTIGATIONAL MEDICINAL PRODUCTS MANUFACTURED IN NON-EU COUNTRIES Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:25 Pharmaceutical industry Health Pharmaceutical sciences Clinical Data Management EudraCT Qualified Person EudraGMP European Medicines Agency Audit Clinical research Pharmaceuticals policy Research
395	NL comment on draft template for the qualified person’s declaration concerning GMP compliance of investigational medicinal products manufactured in non-EU countries March 13, 2013 Reaction Netherlands Ministry of Heal Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:32:47 IMP Template Pharmaceuticals policy Clinical research Qualified Person
396	Warsaw, April 2, 2013 European Commission Directorate General for Health and Consumers, Unit SANCO/D/6 B-1049 BRUSSELS Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:29:55 Clinical research Pharmaceuticals policy Qualified Person
397	22nd March[removed]Submission of comments on European Commission Template for the Qualified Person’s declaration concerning GMP compliance of investigational medicinal products manufactured in Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:29:57 Pharmaceuticals policy Pharmacology Pharmaceutical industry Qualified Person European Medicines Agency QP Comment Clinical research Pharmaceutical sciences Research
398	From: Gabriel Bohl [mailto:[removed]] Sent: Thursday, March 28, 2013 6:20 PM To: SANCO PHARMACEUTICALS D6 Subject: QP declaration to be included in CTA - draft for consultation Quintiles - CRO - large s Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:26 Clinical research Food safety Good manufacturing practice Computing Qualified Person Audit Illkirch-Graffenstaden QP Pharmaceuticals policy Software Pharmaceutical industry
399	European Industrial Pharmacists Group response to the consultation on a unique identifier for medicinal products A. CONSULTATION TOPIC N°1: CHARACTERISTICS AND TECHNICAL SPECIFICATIONS OF THE UNIQUE IDENTIFIER Introduct Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:10 Technology Medicine Traceability Serialization Good distribution practice Pharmacy Counterfeit medications Barcode Qualified Person Pharmaceuticals policy Pharmaceutical industry Health
400	Microsoft Word[removed]EMA comments form_IMP_GMP declaration 3rd countries_comments EQPA.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:28 Audit Auditing Clinical research Pharmaceuticals policy Qualified Person

UPDATE