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Pharmaceutics
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231	Guideline on the use of starting materials-intermediates collected from different sources in the manufacturing of biological medicinal products - for publishing Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2013-07-21 06:43:56 Pharmaceuticals policy Pharmaceutics Pharmacology Clinical research Biologic European Medicines Agency Marketing authorization Committee for Medicinal Products for Human Use Good manufacturing practice Pharmaceutical industry Business Pharmaceutical sciences
232	[removed]Federal Register / Vol. 68, No[removed]Friday, September 5, [removed]Notices • Date the Form FDA 483 issued (from the Form FDA 483); • Firm establishment inventory (FEI) Add to Reading List Source URL: www.nthanalytics.com Language: English - Date: 2010-02-09 22:20:52 Pharmaceutics Pharmaceuticals policy Health Quality Clinical research Title 21 CFR Part 11 Form FDA 483 Validation Office of Regulatory Affairs Food and Drug Administration Pharmaceutical industry Pharmaceutical sciences
233	Cytochrome Cytochrome P450 P450 Activity Activity Screening Screening in in Low-Volume Add to Reading List Source URL: www.promega.com Language: English - Date: 2011-01-21 11:31:32 Pharmaceutics High-throughput screening Plate reader CYP3A4 CYP1A2 IC50 Pharmacology Cytochrome P450 Pharmaceutical sciences
234	Brochure More information from http://www.researchandmarkets.com/reports[removed]Generics in Europe Description: Add to Reading List Source URL: www.researchandmarkets.com Language: English Market analysis Generic drug Business Pharmaceutics Pharmaceutical sciences Pharmaceuticals policy Sanofi STADA Arzneimittel
235	C h a p t e r 1 Pharmaceutical Industry Overview 1.1 Introduction 2 Add to Reading List Source URL: support.sas.com Language: English - Date: 2014-03-05 08:00:41 Pharmaceutical sciences Pharmaceutics Food and Drug Administration Pharmacology Clinical Data Management Validation Clinical Data Interchange Standards Consortium Clinical trial SAS Pharmaceutical industry Clinical research Research
236	HTGH CMDh GUIDANCE DOCUMENTS Published on CMDh Website (http://www.hma.eu/cmdh.html) Documents Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-01-08 10:43:11 Research Pharmaceutics Pharmaceutical sciences Clinical research European Medicines Agency Pharmaceutical industry
237	Information note 16 January 2015 Update - Failure to comply with good clinical practice Bioequivalence studies conducted by GVK Bio 1 Add to Reading List Source URL: apps.who.int Language: English - Date: 2015-01-16 06:07:32 Pharmaceutical sciences Pharmaceutics Pharmacology European Medicines Agency Bioequivalence Clinical trial Clinical research Research Pharmaceutical industry
238	Microsoft Word[removed]en.doc Add to Reading List Source URL: www.admin.ch Language: English - Date: 2014-11-24 04:31:05 Science Pharmaceutical sciences Pharmaceutics Quality management Audit Verification and validation Clinical trial South African National Accreditation System Pharmaceutical industry Good Laboratory Practice Organisation for Economic Co-operation and Development
239	Research Coordinator CV Surgery Clinical Research (FT-R[removed]COMPANY SUMMARY The mission of the Texas Heart® Institute is to reduce the devastating toll of cardiovascular disease through Add to Reading List Source URL: www.texasheart.org Language: English - Date: 2015-01-06 13:50:33 Clinical research coordinator Science Pharmaceutics Clinical trial Clinical Trial Portal Clinical research Pharmaceutical industry Research
240	YOUR P EER -R EVIEWED G UIDE TO G LOBAL C LINICAL TRIALS M ANAGEMENT Add to Reading List Source URL: images.alfresco.advanstar.com Language: English - Date: 2014-11-25 01:42:21 Pharmaceutics Health Clinical trial CenterWatch Clinical research coordinator Pharmaceutical industry Clinical research Research

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