Clinical Trial auditing - identifying risks and building a more compliant and successful trial - Cli (Clinical Trial audit)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: May 20, 2011 End Date/Time: May 20, 2011
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Why Should You Attend:

With the growth of the Pharmaceutical and Biotechnology industry, audits get more and more frequent. Noncompliance in clinical trials and misreporting of clinical trial results that took place in the last years made the regulatory bodies to multiply the number of audits. On the other part, the sponsors also multiplied the audits from their part in the idea to try to downsize the risk of noncompliance during the trial.

This clinical trial audit webinar will help with preparing the site and the study team with how to successfully prepare for an audit, how to identify risk of noncompliance, what to do before, during and after an audit. The session will give you practical solutions to get the best results from an audit and the opportunity to grow the image of your team and/or your site. This session will include the key principles of audit preparation, GCP as defined by the ICH as well as incorporate FDA regulatory inspection strategy to identify areas of common deficiency.

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.


Online Event
2600 E. Bayshore Road
Palo Alto
United States