Web Seminar Recordings on Key Clinical Research Topics
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Archive: Preparation, Management, and Response to Inspections and Audits
Course Description
Faced with an impending audit or inspection, how do you prepare? If inspection results in findings, do you have the skills and tools to best respond to these issues to avoid further actions? This web seminar will provide an overview of what to expect and how to prepare for an audit or inspection. Real case scenarios in a workshop format will be used to help solve the dilemmas faced by both sites and industry when faced with discoveries from regulatory authorities or auditors. Steps for preparation, on-site auditing and follow-up actions will be explained. Interactive exercises will be incorporated utilizing FDA Warning Letters. Participants will learn how to perform root cause analysis (RCA) and prepare corrective and preventive actions (CAPAs).
Video Preview
Learning Objectives
- Describe the anatomy of a regulatory inspection
- Recognize how to best prepare and manage expectations
- Discuss appropriate strategies for responding to inspection findings and implementing realistic and appropriate corrective and preventive actions (CAPA)
- Employ the right corrective actions to resolve the major and critical inspection findings
Who Should Attend
- Investigators
- Clinical Research Coordinators
- Clinical Research Associates
- Compliance Professionals
- Project Managers and Site Managers
- Quality Assurance Personnel
Instructor
Janet Ellen Holwell, C.C.R.C., C.C.R.A.
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.
