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.
Visitors
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
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
Exhibitors
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