![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 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](https://www.pdfsearch.io/img/f1bd956e0bf5902a158fce2176e5eac0.jpg) Date: 2015-12-07 16:54:46Medical 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 PractAdd to Reading ListSource URL: www.transceleratebiopharmainc.comDownload Document from Source Website File Size: 67,52 KBShare Document on Facebook
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