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Good Clinical Practice
Results: 1284

#	Item
151	Information for Participants Registration 2F, Sapporo Convention Center Date Opening Hours Add to Reading List Source URL: www.mwp2014.com Language: English - Date: 2014-10-15 06:07:12 Health Science Design of experiments Pharmacology Medical statistics Clinical trial Institutional review board Good Clinical Practice Good manufacturing practice Clinical research Research Pharmaceutical industry
152	Attachment to Technical Bulletin – AugustDESIGNATED PLAYER When using a designated player (DP) 1. Add to Reading List Source URL: www.nt.softball.org.au Language: English - Date: 2014-03-11 21:31:46 Health Science Design of experiments Pharmacology Medical statistics Clinical trial Institutional review board Good Clinical Practice Good manufacturing practice Clinical research Research Pharmaceutical industry
153	Consultation Paper Proposed clinical trial regulatory arrangements under the Australia New Zealand Therapeutic Products Authority (ANZTPA) Add to Reading List Source URL: www.anztpa.org Language: English - Date: 2014-07-18 01:53:05 Health Science Design of experiments Pharmacology Medical statistics Clinical trial Institutional review board Good Clinical Practice Good manufacturing practice Clinical research Research Pharmaceutical industry
154	Framework for Monitoring: Guidance for the national approach to single ethical review of multi-centre research January 2012 © Commonwealth of Australia 2011 Add to Reading List Source URL: health.qld.gov.au Language: English - Date: 2013-10-01 02:32:33 Health Pharmaceutical industry Design of experiments Pharmacology Medical ethics Institutional review board Clinical trial Medical research Good Clinical Practice Clinical research Research Science
155	CL2001R0999EN0350010.0001_cp 1..2 Add to Reading List Source URL: www.dardni.gov.uk Language: English - Date: 2013-06-03 09:11:14 Clinical research Medicine Bovine spongiform encephalopathy European Union Council Implementing Regulation (EU) No 282/2011 Good Laboratory Practice Pharmaceuticals policy Health European Union directives
156	In the Patient’s Interest: Improving Access to Clinical Trial Data August 2014 Prepared by: Brenda J. Huneycutt, PhD, JD, MPH; Add to Reading List Source URL: avalere-health-production.s3.amazonaws.com Language: English - Date: 2014-09-02 10:04:47 Medicine Pharmaceutical industry Design of experiments Epidemiology Medical statistics Clinical trial Randomized controlled trial Good Clinical Practice Clinical data management Clinical research Research Health
157	APAC GRegiP Policy Document APAC RA-EWG APAC Good Registration Practice (GRegiP) Policy Document Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2014-06-26 21:25:05 Environmental Working Group Regulatory requirement New Drug Application Research Health Pharmacology Clinical research Pharmaceuticals policy Drug safety
158	BENCHMARKING OF EUROPEAN MEDICINES AGENCIES Add to Reading List Source URL: www.hma.eu Language: English - Date: 2013-02-28 05:41:32 Health Clinical research Drug safety Strategic management Pharmacovigilance European Medicines Agency Benchmarking Good manufacturing practice Pharmaceutical sciences Pharmaceutical industry Pharmacology
159	March 26, 2015 CITI-Canada Update CITI-Canada is an online clinical research training program that incorporates the International Conference on Harmonization - Good Clinical Practice (ICH-GCP), Tri-Council Policy Stateme Add to Reading List Source URL: www.aihealthsolutions.ca Language: English - Date: 2015-03-26 18:07:31 Good Clinical Practice Pharmaceuticals policy Dangerous goods Citigroup Regulatory requirement Economy of New York City Economy of the United States Health Clinical site Clinical research pharmacology Pharmaceutical industry
160	PRESS RELEASE Lisbon, Portugal, November 2014 The International Conference on Harmonisation (ICH) Steering Committee (SC) and its Expert Working Groups (EWGs) met in Lisbon, Portugal, EU on November 8 – 13, 2014. The m Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-12-02 06:07:25 Pharmaceuticals policy Pharmaceutical sciences Health Clinical Data Management Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document Common Technical Document Good Clinical Practice Clinical research Research Pharmaceutical industry

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