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ICH GCPs and the Clinical Research Process (Including Phase 0,1,2,3 and Phase 4 trials)
This Webinar is over| Date | Aug 12, 2014 |
| Time | 12:00 PM EDT |
| Cost | $175.00 |
|
Online
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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:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com
CLICK HERE
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
- Clinical Personnel
- Regulatory Affairs Personnel
- Research Personnel
- Quality Personnel
- Manufacturing Personnel
- Legal Personnel
- Personnel who require an understanding of the ICH GCP
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com
CLICK HERE
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