Right Submission at the Medical Device Technology Exchange Conference and Exhibit in Seacaucus, NJ

Right Submission and Greenlight Guru will be hosting a workshop, 510(k) Best Practices: Applying Risk Management and Design Controls. 

In this workshop you will learn a step-by-step approach for identifying the regulatory pathway, testing requirements and verifying these requirements before you even begin your testing. This is all part of an integrated approach to planning of design and risk management for medical devices.

You can learn more about the workshop, and register for the event, by clicking here.