How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls

The Corrective and Preventive Action (CAPA) subsystem is the heart of a medical device's quality management system.

And yet, year after year, CAPA violations are the most frequently observed Quality System subsystem cited by FDA.

Quality teams often stumble with poor root cause determination, reactive approaches, poorly defined CAPA procedures, and the list goes on.

Learn how to avoid these common CAPA pitfalls in this free 60-minute webinar presented by 20+ year medical device industry veteran, Jon Speer, founder and VP of QA/RA at Greenlight Guru.

Follow along as Jon walks you through proven best practices that will improve your CAPA processes, while sharing tactical approaches you can start taking today to ensure the medical devices you design, develop, manufacture and market are safe and effective, for end users and in the eyes of regulators.

Implementing a robust and modern CAPA system will enable your shift from reactionary methods to investigate issues and events to a proactive approach to address potential areas of concern and nip it in the bud.

+ FREE CONTENT BONUS: Registrants will receive these exclusive content downloads following the live event: Step-by-Step CAPA Flowchart and PDF of our eBook on The Ultimate Guide to CAPA.

Watch the webinar

9-17-20 webinar graphic
Specifically, this webinar will cover:
  • Regulatory requirements for CAPA
  • How to avoid the most common CAPA pitfalls
  • How CAPA connects to your other QMS processes
  • Impact of risk management on CAPA
  • How to take a proactive approach to catch issues before they happen
  • Visual demonstration of a modern CAPA system and how it should function
  • Q&A session
Who Should Attend?
  • R&D Engineers and Management
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • Medical Device Executives
  • Clinical Affairs Professionals and Management
Register Now  

Hosted by

Moderator/Presenter: Jon Speer

Founder, Greenlight Guru


About Greenlight Guru

Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.

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