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Pharmaceutical Research
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#	Item
201	Technical User Guide eAF hum-vet version20151001-clean Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:01 Medical research Health Pharmaceuticals policy Clinical research Pharmaceutical industry European Union Pharmacopoeias European Medicines Agency European Pharmacopoeia Marketing authorization Electronic common technical document Adobe LiveCycle
202	Protocol reviewed: Review completed by: Protocol #: Title: Name: Date: Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:51 Medical research Clinical research Pharmaceutical industry Health Food and Drug Administration United States Public Health Service Case report form Adverse event Institutional review board Clinical research coordinator
203	An International Conference on Developing Quality Systems in Health Research: Towards Better Human Subject Protection Udon Thani, Thailand* Charoensri Grand Hotel November 28-29, 2007 Add to Reading List Source URL: www.fercap-sidcer.org Language: English - Date: 2010-02-27 17:52:18 Medical research Design of experiments Health Research Clinical research Pharmaceutical industry Institutional review board Clinical trial Public Responsibility in Medicine and Research
204	Institutional Review Board . ... . . Add to Reading List Source URL: research.missouri.edu Language: English - Date: 2016-02-04 11:59:13 Accountability Medical research Administration Public records Ethics Design of experiments Clinical research ethics Pharmaceutical industry Institutional review board Records management Food and Drug Administration Grant
205	Parking Validation Programs Frequently Asked Questions (FAQs) Q: What are the different types of validations offered? A: Downtown, Cinema and Tech Museum validations. Q: Which garages participate in each validation progr Add to Reading List Source URL: parksj.org Language: English - Date: 2015-09-26 00:20:39 Pharmaceutical industry Validity Clinical data management Clinical research Quality Validation Parking
206	ANNEX 2 Form AFAPPLICATION FORM for RESUBMITTED PROTOCOL REVIEW Protocol Number (To be assigned by REBH member secretary): ... Protocol Title: ... Add to Reading List Source URL: www.health.gov.bt Language: English - Date: 2016-07-05 05:03:16 Medical research Clinical research Pharmaceutical industry Clinical trials Medical ethics Informed consent Principal investigator Clinical research coordinator
207	Microsoft PowerPoint - Southern Presentation CAMD.pptx Add to Reading List Source URL: camd.lsu.edu Language: English - Date: 2010-12-08 16:11:56 Medicine Biology Clinical medicine Cellular senescence Apoptosis Cell signaling Immunology Programmed cell death Assay Chemotherapy In vivo Pharmaceutical Research Institute (PRI)- Albany
208	Zusammenfassung der Master-Thesis von Rossella Belleli Efficiency indicators for new drugs approved by the FDA from 2003 toIn the last decades, the drug development costs have increased while the number of new dru Add to Reading List Source URL: intern.public-health-edu.ch Language: English - Date: 2016-03-01 06:14:39 Pharmaceutical sciences Medical research Pharmacology Pharmaceutical industry Clinical research Drug discovery Clinical pharmacology Food and Drug Administration Drug development Prescription Drug User Fee Act Orphan drug
209	19 JanuaryTransitioning to a compulsory usage of the eAFs for Human and Veterinary procedures 1. Status and next steps (Annex to the HMA eSubmission Roadmap detailing the status and next steps of outlined strategy Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:02 Clinical data management Clinical research Pharmaceutical industry Quality Validation Validity ISO 10303 Electronic submission Knowledge Evaluation Business
210	Microsoft Word - （案3）英語版PMDA Updates4月号.docx Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2016-07-27 04:20:20 Medical research Clinical research Health Pharmaceutical industry Medicine Drug discovery Food and Drug Administration Clinical data management Drug development Clinical trial Validation Medical device