The medical device industry has seen significant regulatory changes in recent years affecting legal and administrative issues, relationships with providers and more.  Members benefit from MDMA’s expertise on compliance issues through interacting with key government enforcement officials, legal experts and other member companies to discuss best practices.

MDMA is also developing a compliance "toolkit” for our members that will include sample governance documents, training documents and auditing documents.

The Compliance Working Group typically meets on the last Tuesday of each month at 2:00pm ET via teleconference. If you would like to join this working group, click here.

Latest News

Global transparency and compliance deadlines for 2018

A timeline of transparency and  compliance deadlines for 2018

MDMA Announces New Vice President and General Counsel

WASHINGTON, DC – The Medical Device Manufacturers Association (MDMA) announced today that Carolyn Bruguera joined the organization... 

MDMA Compliance Toolkit


Upcoming Events

Hogan Lovells Webinar - GDPR for Life Sciences
December 7th  12-1pm Eastern


December Compliance Working Group Roundtable Meeting
December 14th  2pm Pacific

Offices of Wilson, Sonsini, Goodrich & Rosati
650 Page Mill Rd, Palo Alto, CA