The last several years have seen an unprecedented expansion in the roles and responsibilities of medical device professionals. To stay ahead of the curve, quality and regulatory experts need to move out of their comfort zones and familiarize themselves with every stage of the medical device life cycle, from concept, to commercialization, and beyond.

The MEDICAL DEVICE QUALITY ASSURANCE AND REGULATORY AFFAIRS Conference is designed to help senior quality and regulatory leaders overcome challenges related to, harmonization, changing quality standards, and an evolving regulatory landscape by bringing together the top minds in the industry to share
innovations, insights and best practices.

JOIN US in Boston on March 28th and 29th to:

GAIN key insight from senior quality assurance and regulatory affairs professionals from some of America’s largest and most successful medical device companies.

BENEFIT from a unique, market-driven program based on research
with quality assurance and regulatory affairs professionals like you

NETWORK and SHARE best practices with over one hundred
medical device leaders from across North America

RETURN to your office with the tools and the knowledge you need to make rapid and meaningful changes within your organization!

For sponsorship opportunities please contact:
Daniel Gellman
P: 1-877-927-0718 ext. 7389

For media partnership opportunities please contact:
Joanna Chung
P: 1-877-927-0718 ext. 7308

For questions about this year’s program/content, or information on how you can speak next year please contact:
Graeme Thomson
P: 1-877-927-0718 ext. 7290

Venue Information at a Glance

The Colonnade Hotel

120 Huntington Avenue, Boston, MA 02116, USA


To make a reservation at The Colonnade Hotel, please call 617-424-7000 and ask for the best available rate at the time of booking. To book on-line, visit and enter your dates.