GENERAL GUIDELINES FOR INFORMED CONSENT FORMS (ICF)(HREB Health Panel) Please note that a well presented ICF that is in accordance with HREB standards will facilitate the approval process. ICFs that do not adhere to - Reo - Document - PDFSEARCH.IO

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	GENERAL GUIDELINES FOR INFORMED CONSENT FORMS (ICF)(HREB Health Panel) Please note that a well presented ICF that is in accordance with HREB standards will facilitate the approval process. ICFs that do not adhere to Add to Reading List Document Date: 2012-09-12 17:10:58 Open Document File Size: 52,50 KB Share Result on Facebook Country Canada / / Facility University of Alberta / / IndustryTerm food / / Organization University of Alberta / FDA / NCIC/industry sponsor/granting agency / Health Research Ethics Board / / / Position INVESTIGATOR / Principal Investigator / coordinator / researcher / Research/Study Coordinator / / ProvinceOrState Alberta / Oregon / / SocialTag Research Science Design of experiments Pharmaceutical industry Pharmacology Informed consent Research ethics Psychology Internet privacy Clinical research

GENERAL GUIDELINES FOR INFORMED CONSENT FORMS (ICF)(HREB Health Panel) Please note that a well presented ICF that is in accordance with HREB standards will facilitate the approval process. ICFs that do not adhere to Add to Reading List