Medical Device 510k Preparation and Submission Webinar

10 Steps to Preparing Your 510(k) Submission (and How to Avoid the Common Pitfalls)Подробнее

How to Prepare a Medical Device 510k Submission for FDAПодробнее

Refuse to Accept & Additional Information Request: Avoiding Problems with Medical Device SubmissionsПодробнее

Webinar: Medical Devices Cybersecurity in 510(k) Premarket SubmissionsПодробнее

Mastering your 510(k) submission processПодробнее

510(k) eSTAR Webinar - Indications for Use and ClassificationПодробнее

Three 510(k) tipsПодробнее

Using Clinical Data in your 510(k) FDA eSTAR - webinar Feb. 8, 2024Подробнее

Webinar: How PCCP Accelerate Post-Market Updates to AI Algorithms & Device SoftwareПодробнее

Electrical Safety Testing WebinarПодробнее

Using the new eSTAR templates for a 510(k) submission and the FDA eSTAR draft guidanceПодробнее

How to prepare an FDA eSTAR 510(k) submissionПодробнее

510(k) Course Updates for 2022Подробнее

U.S. FDA’s 510(k), IDE, and PMA Documentation, Submission and Approval ProcessПодробнее

Need a medical device 510(k)?Подробнее

Software Validation Documentation for FDA 510(k) pre-market notification submissionПодробнее

Cybersecurity Webinar - Learn what the FDA wants in your 510(k)Подробнее

510(k) Submission Predicate Selection Webinar - Updated for 2022Подробнее

SARACA Free Live Webinar on Roadblocks in the 510(k) Submission ProcessПодробнее

510(k) Project Management - Updated for 2021Подробнее