Description:

Do you know what pitfalls most medical device manufacturers are experiencing as they RUSH to get their devices approved?

• Using old documents and records thinking they will be approved.
• Getting Nonconformance / Deficiency Reports.
• Proper use of Harmonized Standards and Common Specifications.

By attending this webinar you will learn how to help avoid these, and other pitfalls, and make your company’s technical documentation preparation and approval as seamless as possible.

About the presenter:

Markus Gee is our Medical Division Director with 30 years of boots-on-the-ground RA/QA, product development, QMS implementation and right-sizing experience.

Who Should Watch:

Anyone who wants to avoid potential years of setbacks in their MDR transition, including:

• Business Owners
• Quality Managers
• Quality Directors
• Quality Engineers
• Quality Assurance Specialists
• Quality Control Techs
• Internal Auditors
• Supply Chain Managers
• Supply Chain Auditors
• Executives responsible for QMS execution