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Qualified person
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51	INFORMED CONSENT APPLICATIONS IN MUTUAL RECOGNITION AND DECENTRALISED PROCEDURES RECOMMENDATIONS Doc. Ref.: CMDhRev3Rev.4 September 2010 April 2015 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-04-29 06:02:55 Pharmaceutical industry Pharmaceuticals policy Pharmacology Qualified Person for Pharmacovigilance Consent Criminal law Law
52	Annex13 GMPZ herziening 2011 Geneesmiddelen voor onderzoek-na TO Add to Reading List Source URL: www.kennisplein-nvza.nl Language: English Technology Business Science Good manufacturing practice Clinical Trials Directive Validation Good Clinical Practice Directive Qualified Person Packaging and labeling Clinical research Pharmaceuticals policy Pharmaceutical industry
53	Doc. Ref: CMDhRev.1 April 2015 Template for letter of Access for an application under Article 10c of DirectiveEC (‘informed consent’ application) Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-04-29 09:40:20 Qualified Person for Pharmacovigilance Pharmaceuticals policy Drug safety Pharmacology Pharmacy
54	Electronic submission of Articledata_Q&A Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2014-07-09 10:10:55 Clinical research Health Research Drug safety Pharmacy European Medicines Agency EudraVigilance Qualified Person Responsible For Pharmacovigilance Pharmacovigilance Pharmaceuticals policy Pharmacology Pharmaceutical sciences
55	MEMO Add to Reading List Source URL: www.bd.gov.hk Language: English - Date: 2012-03-06 07:01:46 Architect Regulation and licensure in engineering Clinical research Pharmaceuticals policy Qualified Person
56	PROCESS FLOW FOREST LAND GRAZING MANAGEMENT AGREEEMENT (FLGMA) An agreement between a qualified person, association and/or corporation and the government to develop, manage and utilize grazing land. Add to Reading List Source URL: r5.denr.gov.ph Language: English - Date: 2012-11-26 20:27:28
57	PDF Document Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 07:52:05 Pharmacy Health Qualified Person for Pharmacovigilance Pharmacovigilance Pharmacology Pharmaceutical sciences Drug safety
58	GVP Module Safety Communication Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:39:02 Pharmaceutical sciences Pharmacovigilance European Medicines Agency Patient safety Summary of Product Characteristics Adverse effect Qualified Person Responsible For Pharmacovigilance EudraVigilance Medicine Health Pharmacology
59	DOC Document Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 13:01:19 Pharmacy Health Qualified Person for Pharmacovigilance Pharmacovigilance Pharmaceutical sciences Pharmacology Drug safety
60	Microsoft PowerPoint - Bruno - System Master Files 24 aprilCompatibiliteitsmodus] Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 05:09:35 Pharmacy Health Pharmaceuticals policy Pharmacovigilance Qualified Person Responsible For Pharmacovigilance Qualified Person for Pharmacovigilance EudraVigilance Pharmacology Pharmaceutical sciences Drug safety

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