This FDA audit training provides an overview of the audit readiness process from internal evaluation of your quality systems to the logistics of the audit itself; with key emphasis placed on equipping you and your team with the skills needed to present expert testimony during interviews with regulators.
This webinar will provide essential information and a strategy for being in a permanent state of readiness for a regulatory audit. You and every member of your team can benefit by becoming acquainted with the overall audit readiness process and preparing them for the potential of being interviewed by an auditor.
Why Should You Attend:
Pharmaceutical, Medical Device and Biologics industries are subject to oversite inspections by FDA and other regulatory bodies from the geographies where products are marketed. A firm’s successful completion of a regulatory audit is critical to its continued operation and financial viability. Failure can mean delays in product approvals, time consuming and costly remediation efforts and damage to the firm’s reputation for high quality products.This webinar will provide essential information and a strategy for being in a permanent state of readiness for a regulatory audit. You and every member of your team can benefit by becoming acquainted with the overall audit readiness process and preparing them for the potential of being interviewed by an auditor.
Areas Covered in the Webinar:
- The regulatory audit process
- Roles and responsibilities of audit participants
- Preparing to provide expert testimony on your quality system
- Preparing subject matter experts
- Types of audit questions and appropriate answers
- Guising auditors to your quality system’s strengths instead of weaknesses
Learning Objectives:
- Understand the tools needed to accomplish tasks related to regulatory audit readiness
- Understand regulatory authorities’ audit processes
- Understand your role and responsibility during an audit
- Use techniques to establish yourself as an expert in your functional area
- Use techniques to formulate responses to various types of questioning used by FDA and other regulators
- Use strategies for guiding auditors to your quality system’s strengths instead of weaknesses
Who Will Benefit:
- Regulatory Compliance Associates and Managers
- Manufacturing operations managers and associates
- Technical service managers and associates
- R&D managers and associates
- Product mangers
- Project managers
- QA/QC managers
- Documentation
Course Provider
Philip Russ,