FDA-E-CONSENT › Use of an Electronic Informed Consent in Clinical Investigations: Questions and Answers; Draft Guidance for Industry, Clinical Investigators, and Institutional Review Boards

FDA-E-CONSENT - 2015 DRAFT - DRAFT
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Use of an Electronic Informed Consent in Clinical Investigations: Questions and Answers; Draft Guidance for Industry, Clinical Investigators, and Institutional Review Boards


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Document Number

FDA-E-CONSENT

Revision Level

2015 DRAFT

Status

Draft

Publication Date

March 6, 2015

Page Count

12 pages