Classes & Workshops

Investigator Reporting Responsibilities - OHRP

When: Fri., May 18, 10-11 a.m. 2018

Overview: The webinar will also discuss how to make determinations of whether an adverse event is probably related, possibly related, or possibly/probably not related to a drug or device. Why should you Attend: Are you being cited for failure to report safety information, changes to the research plan, or protocol deviations/violations or noncompliance to the sponsor or the IRB?

Price: 150.00

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