MedCity News January 24, 2023
Kristin Havranek, Martin Gomez, Matt Wetzel, Steven Tjoe and Stephanie Philbin

Medtech companies should have a team of FDA advisors at the ready to develop and implement pre- and post-market strategies, prevent and resolve pre- or post-market issues and guide lifecycle management

The ability to collect and leverage data — whether be it from the patient or from provider — is transforming the medtech industry. Consider companies that once largely developed hardware-based products. Now they provide a more comprehensive view of how patients behave.

All of this creates new compliance challenges. How should they address those?

Medtech companies should have a team of FDA advisors at the ready to develop and implement pre- and post-market strategies, prevent and resolve pre- or post-market issues and guide lifecycle management, with a keen understanding...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: FDA, Govt Agencies, Medical Devices
Healthy Returns: Trump’s FDA pick Makary may be a relief for biotech and pharma, analysts say
The telehealth background of Trump's FDA pick: 6 notes
President-elect Trump's picks for CDC, FDA, surgeon general: 31 notes
Opinion: RFK Jr. and MAHA should champion a Marshall Plan for obesity
Trump picks Johns Hopkins surgeon to head FDA: 10 things to know

Share This Article