How to Prepare & Conduct Pre-Submission Meetings
1:15:21
How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls
59:28
Understanding the Power of the FDA Pre-Sub: Tips for a Successful Meeting
1:05:20
How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
33:30
Why you should use Pre-Submission or Q-Sub with FDA?
41:30
Meetings: Pre-submission and Special Programs (4of15) REdI Annual Conference – May 29-30, 2019
40:43
Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program
1:20:11
Preparing Your Technical Documentation under MDR: Proven Tips & Techniques
36:29