Issues with Consent Documents - Webinar By MentorHealth

Date: 27-Mar-13 to 27-Mar-13
Location: Online Training - Webinars / Fremont / California / United States
Category: Healthcare & Pharmaceuticals Conferences & Trade Fairs

Overview: The consent document tends to be the source of much frustration for both research participants, research team members, and the IRB reviewers who must review and approve the document and process before it is implemented.


Principal Investigators / Sub-investigators
Clinical Research Scientists (PKs, Biostatisticians,)
Safety Nurses
Clinical Research Associates (CRAs) and Coordinators (CRCs)
Recruiting staff
QA / QC auditors and staff
Clinical Research Data managers
Human Research Protection professionals


MentorHealth is a comprehensive training source for healthcare professionals. Our trainings are high on value, but not on cost. MentorHealth is the right training solution for healthcare professionals.

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