Pharmaceutical Research

Results: 21355



#Item
191Gaining Trust from Sponsors An Oncology Program Case Study Introduction A biopharmaceutical company chose Cmed to conduct a phase

Gaining Trust from Sponsors An Oncology Program Case Study Introduction A biopharmaceutical company chose Cmed to conduct a phase

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Source URL: www.cmedresearch.com

Language: English - Date: 2016-06-23 04:20:16
192Medical research / Research / Applied ethics / Medical ethics / Clinical research / Design of experiments / Pharmaceutical industry / Institutional review board / Public Responsibility in Medicine and Research / Clinical trial / Human subject research / Informed consent

DOC Document

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Source URL: people.westminstercollege.edu

Language: English - Date: 2009-10-15 14:47:10
193Understanding the European GMO legislation for gene therapy products in clinical trials Jacqueline Barry Director of Regulatory Affairs

Understanding the European GMO legislation for gene therapy products in clinical trials Jacqueline Barry Director of Regulatory Affairs

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Source URL: ct.catapult.org.uk

Language: English - Date: 2016-04-19 09:57:25
194Appendix 1: Agenda Health Informatics Workshop: Use of the electronic health record in the design and conduct of clinical trials 10:00-16:00, Monday 23rd June 2014 Staff House Conference Centre, The University of Manches

Appendix 1: Agenda Health Informatics Workshop: Use of the electronic health record in the design and conduct of clinical trials 10:00-16:00, Monday 23rd June 2014 Staff House Conference Centre, The University of Manches

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Source URL: www.network-hubs.org.uk

Language: English - Date: 2015-07-13 18:17:01
195IRB NON-MED  CONTINUING REVIEW FORM  Last Revision Date:

IRB NON-MED CONTINUING REVIEW FORM Last Revision Date:

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Source URL: humansubjects.stanford.edu

Language: English - Date: 2016-04-12 01:21:51
196Microsoft Word - Subject Registration System Instructions v2Clean

Microsoft Word - Subject Registration System Instructions v2Clean

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Source URL: ictr.research.bcm.edu

Language: English - Date: 2015-01-21 09:40:49
197REFLECTION	
  PAPER	
  -­‐	
  EFPIA	
  Guiding	
  Principles	
  on	
  Layperson	
  Summary	
   	
   EU	
  Clinical	
  Trials	
  Regulation	
  	
  –	
  Annex	
  V	
     	
  

REFLECTION  PAPER  -­‐  EFPIA  Guiding  Principles  on  Layperson  Summary     EU  Clinical  Trials  Regulation    –  Annex  V      

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Source URL: www.efpia.eu

Language: English - Date: 2016-04-05 10:42:36
198402nd OMICS International Conference  Scientific Program Pharmaceutical Summit and Expo

402nd OMICS International Conference Scientific Program Pharmaceutical Summit and Expo

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Source URL: global.pharmaceuticalconferences.com

Language: English - Date: 2015-09-28 02:27:24
199DOD and HSRRB Specific Requirements

DOD and HSRRB Specific Requirements

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Source URL: mrmc.amedd.army.mil

Language: English - Date: 2013-04-16 15:32:17
200Norman M. Goldfarb Career First Clinical Research LLC Managing DirectorPresent) First Clinical Research provides clinical research best practices information, consulting and training services, and publishes the Jo

Norman M. Goldfarb Career First Clinical Research LLC Managing DirectorPresent) First Clinical Research provides clinical research best practices information, consulting and training services, and publishes the Jo

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Source URL: firstclinical.com

Language: English - Date: 2016-06-24 17:31:26