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Pharmaceutical Research
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211	Version Date: Version Date: September 2015 © Horizon Health Network - Ethics Services Internal Working Document Page 2 of 10 Horizon Health Network Research Ethics Board Add to Reading List Source URL: en.horizonnb.ca Language: English - Date: 2015-10-08 09:05:45 Medical research Pharmaceutical industry Clinical research Clinical research coordinator Clinical trial Informed consent Confidentiality Good clinical practice Medical privacy
212	® PREDICT Pharmacological qualification of anticancer agents. DRUG SCREENING, LEAD AND CLINICAL Add to Reading List Source URL: www.oncodesign.fr Language: English - Date: 2014-02-14 04:37:30 Medicine Immunology Medical research Health care Drug discovery Pharmaceutical industry Pre-clinical development In vitro Cytotoxicity Syngenic Antibody In vivo
213	Microsoft PowerPoint - Q10 development [Compatibility Mode] Add to Reading List Source URL: www.biomechanics-coordination.eu Language: English - Date: 2010-12-10 08:32:39 Quality Pharmaceutical industry Validity Clinical data management Clinical research Validation Q10
214	 HOME STUDY Daily Challenges to the Future of Clinical Trial Conduct Challenges and Training Needs for Clinical Research Associates—A Survey Add to Reading List Source URL: www.acrpnet.org Language: English Clinical research Pharmaceutical industry Clinical research associate Clinical trial National Security Agency Monitoring in clinical trials
215	Stanford University What Qualifies as Human Subject Research HRPP Policy Guidance Add to Reading List Source URL: researchcompliance.stanford.edu Language: English - Date: 2016-04-12 01:21:49 Clinical research Pharmaceutical industry Design of experiments Medical ethics Research ethics Clinical trial Human subject research Food and Drug Administration Research Institutional review board Clinical research coordinator
216	EU Module 1 Specification VersionRelease Notes November 2011 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:45 Computer file formats Clinical data management Clinical research Electronic common technical document Pharmaceutical industry Marketing authorization ACE Doc Specification Zip
217	Annex1 - A guide to the filenaming convention for eSubmission Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:00 Pharmaceutical industry Clinical data management Health informatics Agencies of the European Union Clinical research Electronic common technical document European Medicines Agency Marketing authorization ASMF EMA
218	ATTORNEY LISTINGS FINANCE & TRANSACTIONAL LOCATION Jane Adams Add to Reading List Source URL: www.managingip.com Language: English - Date: 2015-09-23 06:23:30 Biotechnology Pharmaceutical industry Drugs Pharmacy Biopharmaceutical Biosimilar Small molecule Pharmaceutical drug Antibody Center for Drug Evaluation and Research Personalized medicine
219	 HOME STUDY Daily Challenges to the Future of Clinical Trial Conduct Drug Products for InvestigatorInitiated Research PEER REVIEWED \| Philip K. Burns Add to Reading List Source URL: www.acrpnet.org Language: English - Date: 2016-03-31 09:50:44 Pharmaceutical industry Clinical research Drug development Validation Food and Drug Administration Good manufacturing practice Clinical trial Verification and validation Investigational New Drug Pharmaceutical drug Drug discovery Quality management system
220	Clinical Trial Associate (MP0125) We are looking for a committed, self-motivated Clinical Trial Associate (CTA) with a strong hands-on attitude to complete our Clinical Operations team. Your responsibilities: Add to Reading List Source URL: www.molecularpartners.com Language: English - Date: 2016-07-21 08:27:34 Clinical research Pharmaceutical industry Clinical trials Trial master file Molecular Partners Good clinical practice

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