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Why are we Seeing More Independent Data Safety Monitoring 

When: Tue., Dec. 5, 10-11:30 a.m. 2017
Phone: 800-447-9407
Email: support@compliance4All.com
Price: $ 150.00
www.compliance4all.com/control/w_product/~product_id=501591LIVE?channel=clevescene_Dec_2017_SEO
Overview: 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.

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