How to Ace your Internal Audits in 2022

There are few times when efficiency, effectiveness, and accuracy are more important for your product and processes than during internal audits. 

What’s more is that regulatory bodies around the world require medical device companies to conduct internal audits.

Still, many medical device companies struggle with internal auditing and the quality of these audits can vary widely.

The purpose of this webinar is to walk you through the best practices for setting up internal audits within your organization so that you’re able to conduct them with ease on a consistent basis.

There’s no better way to kickoff 2022 than by learning proven methods and actionable tips for:

  • How frequently internal audits are recommended to be held
  • How to navigate new changes to ISO 14791:2019
  • What is important for an MDSAP or EU MDR audit
  • How to make sure that you have covered topics like complaint handling and CAPAs

Register for this free, in-depth webinar presented by Kyle Rose of Rook Quality Systems who will provide a detailed explanation of the aforementioned QMS functions, as well as the cross-functional collaboration methods you can use to benefit your product, QA/RA, and engineering teams.


Watch the webinar

K.Rose webinar 1-13-22 promo graphic
Specifically, this webinar will cover:
  • Importance of conducting audits
  • Balancing the issue of frequency
  • Internal auditing for Design Control / Risk Management (ISO 14971)
  • Internal auditing for MDR / MDSAP
  • Internal auditing for CAPAs / Complaints
Who Should Attend?
  • Medical Device Executives
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • Clinical Affairs Professionals and Management
  • R&D Engineers and Management
Register Now  

Hosted by

Presenter: Kyle Rose

President, Rook Quality Systems

Taylor Brown
Moderator: Taylor Brown

Senior Medical Device Guru, Greenlight Guru


About Rook Quality Systems

Rook Quality Systems provides specialized and custom consulting services for all classes of medical devices. We work with you to outline your quality and business goals to develop innovative and efficient practices that improve compliance and profit. You can see a full list of the service offerings from Rook Quality Systems by visiting their website to learn more.


About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

Featured In