MDMA 2022 FDA Forum

Date: 9-10 March 2022

Location: Virtual

Laurie Clarke is attending the 2022 FDA Forum hosted by the Medical Device Manufacturers Association (MDMA). Meet with Laurie in advance of the event.

MDMA is hosting their most popular event, the FDA Forum, virtually this year. The event is scheduled for 9-10 March. This year’s forum will focus on the latest strategies and insights governing the 510(k) and PMA regulatory pathways.

Laurie Clarke, TSG’s VP of Medical Device Regulatory, will join FDA officials, device industry representatives, and other FDA regulatory professionals in sharing information about FDA’s current and planned regulation of medical devices, as well as the Agency’s COVID-19 efforts.

Interested in speaking with Laurie in advance of the event? Have questions about the evolving regulatory landscape for 510(k), de novo, and PMA submissions? Contact info@tsgconsulting.com and we will be happy to put you in touch with Laurie.   

Contact us