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Good Clinical Laboratory Practice
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1	The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia has prepared the unofficial consolidated text for the Medicinal Products Act which includes:  Medicinal Products Act (Official Gazette Add to Reading List Source URL: www.jazmp.si Language: English - Date: 2013-07-12 06:13:47 Pharmaceuticals policy Health Medical research Clinical Trials Directive Directive 2001/83/EC Good laboratory practice Marketing authorization Good Clinical Practice Directive European Pharmacopoeia Biopharmaceutical Pharmacovigilance European Medicines Agency
2	Code of Practice for the Promotion of Animal Medicines Together with the Rules of Procedure for the Add to Reading List Source URL: www.noah.co.uk Language: English - Date: 2016-04-25 10:46:34 Health Pharmaceutical sciences Pharmacy in the United Kingdom Executive agencies of the United Kingdom government Veterinary Medicines Directorate Clinical pharmacology Pharmaceuticals policy European Medicines Agency National Office of Animal Health Good laboratory practice Summary of Product Characteristics Paraveterinary workers
3	IRIS PHARMA FACT SHEET A GLOBAL SERVICE PROVIDER OF PRECLINICAL AND CLINICAL RESEARCH IN OPHTHALMOLOGY KEY FACTS COMPANY OVERVIEW Add to Reading List Source URL: www.iris-pharma.com Language: English - Date: 2016-07-21 07:47:37 Pharmaceutical industry Clinical research Drug discovery Contract research organization Pre-clinical development Good laboratory practice Drug development Vision Institute Clinical trial Ophthalmology Medicine Draft:BertinPharma
4	Rules on the Medicines Act Add to Reading List Source URL: oag.gov.bt Language: English - Date: 2015-04-15 23:30:42 Pharmaceutical industry Pharmaceuticals policy Food and Drug Administration Clinical trial Design of experiments Product testing Good laboratory practice Marketing authorization European Medicines Agency
5	R: Regulatory Compliance and Validation Issues A Guidance Document for the Use of R in Regulated Clinical Trial Environments December 15, 2014 Add to Reading List Source URL: www.r-project.org Language: English - Date: 2015-03-04 04:31:16 Pharmaceutical industry Validation R Title 21 CFR Part 11 Good laboratory practice Medical device Good manufacturing practice Clinical trial Business process management Software Electronic trial master file
6	Microsoft Word - Code of Ethics Add to Reading List Source URL: www.embs.org Language: English - Date: 2015-12-11 09:17:55 Clinical research Medical ethics Research ethics Good laboratory practice Organisation for Economic Co-operation and Development Human subject research Pharmaceutical industry
7	NATIONAL PROGRAMME Chapter 6 Agriculture Add to Reading List Source URL: www.translation-centre.am Language: English - Date: 2008-10-07 01:30:11 Health Technology Clinical research Food safety Product safety Prevention Directive 93/41/EEC Good Laboratory Practice Pharmaceuticals policy Packaging European Union directives
8	Microsoft Word - Enf Strategy Finaldoc Add to Reading List Source URL: www.communityequipment.org.uk Language: English - Date: 2013-08-14 04:27:52 Clinical research Pharmaceutical sciences Department of Health Medicines and Healthcare products Regulatory Agency Pharmaceuticals policy European Directive on Traditional Herbal Medicinal Products Medical device Good Laboratory Practice Regulation of therapeutic goods Medicine Pharmaceutical industry Health
9	mvi_header_factsheet-blue Add to Reading List Source URL: www.malariavaccine.org Language: English - Date: 2011-11-10 13:38:17 Vaccines Montgomery County Maryland Walter Reed Army Institute of Research Malaria vaccine ELISA Plasmodium falciparum Good Clinical Laboratory Practice Medicine Malaria Health
10	2004R0882 — EN — — — 1 This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents ►B REGULATION (EC) NoOF THE EUROPEAN Add to Reading List Source URL: www.fsai.ie Language: English - Date: 2012-01-04 09:29:36 Health Medicine European Union Good Laboratory Practice Directive 93/41/EEC Pharmaceuticals policy European Union directives Clinical research

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