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Thu - Dec 1, 2011 @ 12:00 PM CST Ended
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The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - Barriers and Solutions

(complianceonline.com)

This GCP/ICH regulations training will focus on the regulatory requirements that Sponsors, Monitors, and Investigators must follow to be GCP compliant.

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 29th November 2011.

Tags

  • Clinical trial compliance training, clinical research compliance, GCP compliance, good clinical practices compliance training, GCP ICH guidelines, clinical research sponsors obligations, clinical rese

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