This webinar discusses how to improve the informed consent process for subjects enrolling in clinical research. It focuses on the process used to deliver information to subjects over the consent document itself. The webinar concludes with the challenges related to informed consent and summarizes potential strategies to use for improvement by researchers and IRBs.
Note: Attendees should have a basic knowledge of the regulatory requirements and ethical principles for informed consent as a prerequisite for this webinar.
Language Availability: English
Suggested Audiences: Clinical Research Coordinators, Contract Research Organizations (CROs), Investigators, IRB Members, Key Study Personnel, Research Nurses, Research Staff who are Involved in the Design and Conduct as well as the Oversight and Management of Clinical Trials with Drugs and/or Biologics, Sponsors
Organizational Subscription Price: $300 per year/per site or included as part of the $1,000 annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person