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ICH GCPs and the Clinical Research Process Including Phase 0123 and Phase 4 trials

8/12/2014 10:00 AM - 11:30 AM

Overview:

This webinar provides all the necessary information concerning the ICH GCP-the only global GCP. ICH GCP is not only the only global GCP it is also the most current GCP. If you are involved with clinical trials the ICH GCP is a must for you.

This webinar presents a comprehensive overview of the ICH GCP and other clinical requirements for conducting clinical trials. Learn about the ICH GCP, use of the ICH GCP during clinical trials and the general concepts upon which clinical trials are based. This webinar allows clinical professionals to prepare for and conduct clinical trials.

Why Should You Attend:

This webinar is a must for those who need to know how to properly conduct a clinical trial. Clinical trials must be conducted according to Good Clinical Practices (GCP). This webinar will inform you about which GCP to use and provide all the necessary information about the GCP.

Areas Covered in the Session:

Learn about the ICH GCP

Learn about human clinical trials

Learn about IRB Obligations

Investigator Obligations

Sponsor Responsibilities

Who Will Benefit:

Clinical Personnel

Regulatory Affairs Personnel

Research Personnel

Quality Personnel

Manufacturing Personnel

Legal Personnel

Personnel who require an understanding of the ICH GCP

Quick Contact:

GlobalCompliancePanel

USA Phone:800-447-9407

Fax: 302-288-6884

webinars@globalcompliancepanel.com

http://www.globalcompliancepanel.com

Event Link - http://bit.ly/1m1ouoi

Learn More: ICH GCPs and the Clinical Research Process Including Phase 0123 and Phase 4 trials

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