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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
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

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

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Source URL: www.transceleratebiopharmainc.com

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File Size: 67,52 KB

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