Microsoft Word - AID-C1_consent_form_tips_Rev2.docx - Experiments - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2016-08-02 13:55:17 Medical ethics Clinical research ethics Human subject research Clinical research Design of experiments Informed consent Institutional review board Consent Clinical trial Health Insurance Portability and Accountability Act Treaty		Microsoft Word - AID-C1_consent_form_tips_Rev2.docx Add to Reading List Source URL: researchcompliance.stanford.edu Download Document from Source Website File Size: 312,29 KB Share Document on Facebook

	Human Subjects PROTECTIONS Training Certification Training in Human Research Subject Protections is required for all individuals who are participating in research activities at Children’s Hospital & Research Center Oak DocID: 1uyry - View Document
	2.8 Human Subject Research Specimens Page 1 of 2 UTMB Office of Clinical Research Standard Operating Procedure 2.8 Human Subject Research Specimens DocID: 1tIUe - View Document
	2.2 Pre-screening for Human Subject Research Page 1 of 1 UTMB Office of Clinical Research Standard Operating Procedure 2.2 Pre-screening for Human Subject Research DocID: 1tICH - View Document
	Stanford University Report Form for Human Subject Investigation RPT-P3 Research Compliance Officeusing Biological Agents or Recombina DocID: 1su3l - View Document
	THE CIRP FRESHMAN SURVEY INFORMATION SHEET PURPOSE OF THE STUDY You are asked to complete this survey as part of a national study conducted by the Higher Education Research Institute (HERI) at the University of Californi DocID: 1rtBt - View Document