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Fri - Dec 16, 2011 @ 12:00 PM CST Ended
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FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program

(complianceonline.com)

This FDA Clinical Trial Auditing training will cover the FDA regulations and the ICH GCP recommendations to ensure your site is prepared for a clinical trial audit.

Why Should You Attend:

There is an increasing frequency of real-time FDA Audits of trials and it seems that no one is well prepared.

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 14th December 2011.

Tags

  • Clinical Trial Audits, Due Diligence, FDA Clinical Trial Auditing, IRB PI Protocol, sponsor monitoring system, study contact, Sponsor responsibility, ICH GCP guidelines for trial audit

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