What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness? 2012 is a webinar that covers topics such as:
- Clinical Site Audits/Inspections findings and FDA warning letters
- Audits and Inspections: Definitions, Goals, Causes and Procedures
- Preparation for a planned Audit/Inspection – tools and techniques
- Responsibilities of the sponsor, CRO, Investigational site/Investigator
- Completion and follow up after the Audit/inspection
- Appropriate conduct during the Audit/Inspection
- Implementation of corrective action plan – tools and techniques
- DOs and DON`Ts prior to, during and after an Audit/Inspection
- Ensuring continuous Audit/Inspection preparedness – tools and techniques
What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness? 2012 brings together Clinical Research Personnel in the Biotech, Pharma and Medical Device industries, including:
- Principal Investigators
- Sponsor/CRO/Investigative sites General Managers and Directors
- Project Managers
- Site Coordinators
- Clinical Research Associates / Monitors
- Clinical Team Managers/Leaders
- Clinical Research Trainers
- Project Assistants
- Regulatory Compliance Associates and Managers
- Quality Assurance personnel