Conference Description:
This clinical trial audit training reviews the key elements of quality auditing processes and correlates them to the ICH guidelines and applicable FDA regulations.
This Quality auditing in clinical trial training will include the key elements of quality auditing process, auditing methodology, and reporting techniques. In addition, this session will focus on reviewing recent FDA inspection findings and areas of common deficiencies. It will help you understand how key elements of quality auditing process correlates to ICH guideline and other applicable regulations.
Who Will Benefit:
This webinar will provide valuable assistance to all personnel in: Pharmaceutical, Biotechnology, Medical Devices, and Research Facilities Conducting Clinical Trials including:
- Managers in clinical development
- Quality assurance managers and auditors
- Investigator’s site management
- Clinical Operations and study conduct staff
- Regulatory Compliance associates and managers
Start Date: 2010-09-29
Last Day: 2010-09-29
Contact Person: admin
Email: admin@complianceonline.com
Address:
2600 E. Bayshore Road, Palo Alto, CA, 94303, United States
Tel: 650-620-3915
Fax: 650-963-2556
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