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491	College ter Beoordeling van Geneesmiddelen © Certiked ONDERZOEKSVERSLAG Rapportage van de toetsing van het kwaliteitsmanagementsysteem van Add to Reading List Source URL: www.cbg-meb.nl Language: Dutch - Date: 2015-04-17 03:13:42
492	Microsoft Word - Tweetalig advies Resveratrol II v2 Add to Reading List Source URL: www.cbg-meb.nl Language: Dutch - Date: 2015-04-17 02:41:24
493	Microsoft Word - certiked rapport ENG-2012_MdC Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 21:04:36 Auditing Quality Drug safety Pharmacology Pharmacovigilance Pharmacy Internal audit Audit ISO Risk Management Evaluation
494	Microsoft Word - xs02!.DOC Add to Reading List Source URL: www.cbg-meb.nl Language: Dutch - Date: 2015-04-17 08:09:04
495	Overzicht verleende vergunningen voor het bereiden, verpakken, etiketteren of afleveren van diergeneesmiddelen. Nummer Add to Reading List Source URL: www.cbg-meb.nl Language: Dutch - Date: 2015-04-17 07:41:52
496	Microsoft Word - 2nd opinion rapeseed protein NL bilingual Add to Reading List Source URL: www.cbg-meb.nl Language: Dutch - Date: 2015-04-17 00:27:24
497	Microsoft PowerPoint - Anja - articleapril 2012 Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 14:33:14 Data Information Radio-frequency identification ISO/TC 215 Registration authority Metadata Data element Enterprise application integration
498	LEN Official Journal of the European Union Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 21:10:33 Biology European Union directives Law Genetic engineering Council Implementing Regulation (EU) No 282/2011 Supplementary protection certificate European Union law European Commission number Genetically modified organism
499	PDF Document Add to Reading List Source URL: www.cbg-meb.nl - Date: 2015-04-17 21:06:59
500	PDF Document Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-16 23:41:56 Pharmaceutical industry Health Pharmaceutical sciences European Medicines Agency European Union law Test data exclusivity EudraLex Electronic Common Technical Document Clinical research Pharmaceuticals policy Research

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