Webinar Replay: Waiving or Altering Consent for Minimal Risk Trials

FDA regulations and the Common Rule share the same definition for “minimal risk,” but while the Common Rule allows a waiver of informed consent for minimal risk research if specific criteria are met current FDA regulations do not. Webinar Replay expires July 11, 2019.

Webinar Replay: ICH GCP E6 (R2) – An Overview

This free recorded webinar reviews recent changes to Good Clinical Practice guidelines, including those affecting investigator responsibilities, sponsor responsibilities, essential documents, and more.