Clinical Compliance 2012 - How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices
Date2012-03-20
Deadline2012-03-20
VenuePalo Alto, USA - United States
KeywordsGCP Requirements; CAC Requirements; Systematic; Integrative Compliance; ICH-GCP guidelines; ISO 14155; Enforcement actions; clinical trials; IRBs; adverse event reporting
Topics/Call fo Papers
This 90-minute webinar will help you establish an effective Good Clinical Practice (GCP) by providing a current, accurate and complete (CAC) review and understanding of the relevant and applicable regulations for clinical trials or studies, the requirements and compliance in a systematic, integrative (SI) manner.
Why Should You Attend:
To be able to achieve sustainability and to remain sustainable and competitive in global medical product markets, it is necessary to streamline regulatory compliance processes, in particular, the Good Clinical Practice (GCP) for clinical trials and studies and beyond.
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Last modified: 2012-02-10 15:44:58