Pharmaceutical Research - PDFSEARCH.IO - Document Search Engine

Pharmaceutical Research
Results: 21355

#	Item
381	DD_Brochure_Layout:17 AM Page 3 Do More Trials DD_Brochure_Layout:17 AM Page 4 Add to Reading List Source URL: www.drugdev.com Language: English - Date: 2015-10-27 13:59:32 Clinical research Pharmaceutical industry Clinical pharmacology Clinical trials Clinical trial Design of experiments Medidata Solutions Clinical trial portal
382	Emil Fischer Graduate Programme of Pharmaceutical Sciences and Molecular Medicine Sprecher: Prof. Dr. M. Heinrich, Lehrstuhl für Pharmazeutische Chemie DFG Research Training Group 1910 Add to Reading List Source URL: www.grk1910.de - Date: 2016-04-12 10:29:23
383	DrugDev_DrivingROI_Layout:55 PM Page 1 Driving ROI: The Case for Investing in Global Site Payment Services Add to Reading List Source URL: www.drugdev.com Language: English - Date: 2015-09-08 16:27:46 Medical research Health Clinical research Pharmaceutical industry Healthcare reform in the United States Clinical trial Design of experiments Drug discovery Bundled payment
384	Protocol ID: PD: Meeting Date: Protocol Title: Checklist completed by (IRB Staff name): Date: Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-02-06 14:47:15 Medical research Research Medical ethics Design of experiments Health Clinical research Pharmaceutical industry Clinical trial Institutional review board Health Insurance Portability and Accountability Act Health insurance Experiment
385	Regulatory Science Bootcamp “Clinical Trials Hurdles: Where are they and what should we do?” AGENDA Add to Reading List Source URL: www.icts.uci.edu Language: English - Date: 2015-10-05 15:48:46 Clinical research Pharmaceutical industry Clinical trials Trial master file
386	Match and Master Data to Predict Site Success Selecting the right investigators and sites to run your trial is a critical success factor which directly impacts enrollment, patient retention, data integrity, study timelin Add to Reading List Source URL: www.drugdev.com Language: English - Date: 2015-09-08 16:27:49 Medical research Clinical research Clinical trials Pharmaceutical industry Clinical data management Contract research organizations Clinical trial Patient recruitment Investigator Clinical trial portal ViS Research
387	Stanford University HRPP Informed Consent Checklist Medical Research, Clinical Investigations CHK-C1m 1/4 Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-06-26 16:17:02 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Clinical trial Title 1 of the Code of Federal Regulations Health Insurance Portability and Accountability Act Informed consent
388	Informed consent information should be consistent with procedures, etc. as described in eProtocol application VA research: Refer to CHK-7 VA Research and AID-27m Reviewing VA Research for additional requirements Regul Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2014-08-06 19:30:22 Medical research Clinical research Clinical research ethics Pharmaceutical industry Medical ethics Design of experiments Title 1 of the Code of Federal Regulations Clinical trial Health Insurance Portability and Accountability Act Informed consent
389	Wayne K. Anderson Curriculum Vitae EDUCATION: University of Wisconsin, Madison, Wisconsin: Ph.D. in Pharmaceutical Chemistry; University of Wisconsin Research Foundation Fellow Add to Reading List Source URL: ahc.buffalo.edu Language: English - Date: 2015-02-27 08:27:35
390	Minimum Criteria for ICH E6 GCP Investigator Site Personnel Training (Excerpt from TransCelerate BioPharma Operating Principles) Scope The intent of this document is to define the Minimum Criteria for Good Clinical Pract Add to Reading List Source URL: www.transceleratebiopharmainc.com Language: English - Date: 2015-12-07 16:54:46 Medical research Clinical research Pharmaceutical industry Good clinical practice Adverse event Source document Public Responsibility in Medicine and Research Informed consent Inclusion and exclusion criteria Serious adverse event Human subject research Trial master file