An Introduction to Complaints, Nonconformance and CAPA

An Introduction to Complaints, Nonconformance and CAPA

Cancel Apply

rate limit

Code not recognized.

The Risk Management Process and ISO 14971
The Risk Management Process and ISO 14971
This course will describe the role of risk management in the industry, explain the framework of the risk process, and define many key terms you'll need to know.
0 hr 32 min
Risk Management Ideation & Prototyping Product Development QMS Refinement & Regulatory Submissions Product Launch Advance Exclusive Course
What is the Best Way to Structure a Risk Management File
What is the Best Way to Structure a Risk Management File
A session by Carolyn Guthrie, Director QA/RA at Kapstone Medical
0 hr 48 min
Initial QMS Procedures Product Development Advance Exclusive Webinar
Risk Management from a Regulatory and Product Development Perspective
Risk Management from a Regulatory and Product Development Perspective
Another favorite podcast episode with our frequent guest Mike Drues, Ph.D.
Risk Management Regulatory Management Product Development QMS Refinement & Regulatory Submissions Advance Exclusive Podcast
Risk Management Plan Template
Risk Management Plan Template
Plan your approach to risk within your quality management system with this helpful template to get you started.
Risk Management Template Advance Exclusive
Pre-Market vs. Post Market Risk: What are the similarities and differences?
Pre-Market vs. Post Market Risk: What are the similarities and differences?
A session by Mike Drues Ph.D., President at Vascular Sciences
0 hr 47 min
Risk Management Product Development QMS Refinement & Regulatory Submissions Product Launch Post-Market Surveillance Advance Exclusive Webinar
How to Integrate Risk Management Throughout the Lifecycle of a Medical Device
How to Integrate Risk Management Throughout the Lifecycle of a Medical Device
Join Greenlight Guru Founder, Jon Speer, as he discusses the next decade of risk in the medical device industry.
Risk Management ISO 14971 Ideation & Prototyping Initial QMS Procedures Product Development QMS Refinement & Regulatory Submissions Product Launch Post-Market Surveillance Advance Exclusive Webinar
ISO 14971 Risk Management for Medical Devices
ISO 14971 Risk Management for Medical Devices
Use this guide to align with the latest version of ISO 14971 and to learn additional tips and insights for medical device risk management.
Risk Management QMS ISO 14971 Ideation & Prototyping Initial QMS Procedures Product Development QMS Refinement & Regulatory Submissions Product Launch Post-Market Surveillance eBook

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.

×
Greenlight Guru Academy specializes in providing education and training resources for medical device professionals.
Education
Content Memberships Certificates
Resources
Templates & Checklists Ebooks & Guides Global Medical Device Podcast GG Medical Device Blog Glossary Partner Directory
Events
Calendar Webinars True Quality Roadshow
Training
GG QMS Partners Gators
Help
Contact Support Advisory Services Guru Edge Sales