Preparing for FDA Inspection and Handling the Consequences 2012 is a webinar that covers topics such as:
- Discussion on receiving and responding to 483s and warning letters
- Preparing for an FDA Inspection
- Discussion on what actions the FDA can take over and beyond issuing a 483 or Warning Letter
Preparing for FDA Inspection and Handling the Consequences 2012 brings together:
- Project Managers
- Clinical Research managers
- Monitors
- Clinical Research Associates
- Research coordinators
- Quality Assurance Professionals
- Clinical investigators
