Live Webinar: Streamlining your Internal Auditing Program for FDA and ISO 13485 Compliance When: Friday October 22, 2021 - 03:00 PM Duration: 60 Minutes.
This presentation will provide an understanding of the entire internal auditing process to efficiently meet the requirements and expectations of the FDA and ISO 13485 Notified Body auditors. Internal audits often get put off or just run through the same old thing every year. But a good auditing program can add value to the company. A well-planned audit program conducted by independent trained auditors will find problems before regulatory auditors do, and also before they become costly mistakes for the company. This webinar will cover how to plan the audit system and how to plan a realistic annual internal audit schedule that covers all the requirements of your company’s quality system.
This webinar will provide the information you need to know to:
Develop or update and internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485
Manage an Internal Audit system , Understand the difference between internal and external audits
Learn how the internal auditing system can add value to your quality system and your company
Areas Covered in the Session:
Develop or update a risk-based internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485
Manage an Internal Audit system
Understand the difference between internal and external audits
Learn how the internal auditing system can add value to your quality system and your company
Understand what makes a good internal audit
Understand the skill required for an internal auditor
Register soon because space is limited.
We hope you’re able to join us!