Netzealous LLC DBA - Compliance4All, Online
It is important to see what the FDA regulations and the ICH GCP recommendations are in regard to DMC's. Most importantly, when does an adverse event (AE) or string of AE's lead to changes in a study protocol or even discontinuation of a study.
Why should you Attend:
With the increasing requirements for a DMC oversight it behooves all involved to know the set-up and function of these committees. Forewarned is forearmed.
Areas Covered in the Session:
Studies requiring a formal Safety Monitoring Committee
What does the "Charter" of a DMC compose of?
What is the composition and function of a DMC?
What types of studies "require" a DMC?
Who Will Benefit:
Clinical Research Scientists
Clinical Research Associates (CRAs)
Event Fee: One Dial-in One Attendee Price: US$150.00
Compliance4All DBA NetZealous,