-
Introduction 0 hr 1 min
- Course Content
-
An Overview of CAPA 0 hr 15 min
-
Knowledge Check
- Summary
-
Conclusion 0 hr 1 min
Overview of CAPA
The CAPA process is almost always a topic of audits and inspections and regularly one of the top reasons for medical device submissions to be rejected by regulatory bodies. Learn what this process is and why it's so important to creating safer and better medical devices.
This website stores cookies on your computer. These cookies are used to collect information about how you interact with our website and allow us to remember you. We use this information in order to improve and customize your browsing experience and for analytics and metrics about our visitors both on this website and other media. To find out more about the cookies we use, see our Privacy Policy and other Terms and Conditions at https://www.greenlight.guru/legal-info.
×