The premier medical device conference driving the speed of innovation.

Book your hotel by April 4 to save!

Since 2009, MedCon has united regulators and healthcare products industry experts for unparalleled exchanges.

MedCon 2023 is hosted by the AFDO/RAPS Healthcare Products Collaborative and co-sponsored by the Food and Drug Administration (FDA) of the U.S. Department of Health and Human Services. Join us April 24-27 in Columbus for three days of purpose-driven discussions that harmonize different perspectives to inspire collaboration, lead innovation, and make a difference in patient care.

MedCon 2023 by the #s

50

speakers

15

moderators

30+

FDA speakers

26

sessions

4

tracks

An experience like no other!

Reuniting in-person for the first time since 2019, MedCon 2023 will unite global regulators and industry experts for open, candid conversations on the most critical issues.

Full-day risk management pre-conference workshop (April 24; separate registration required) and two-and-a-half-day, in-depth Conference (April 25–27)

Paradigm-shifting dialogue leading to practical solutions that can be implemented immediately

Proactive and predictive methods to protect products, businesses, and patients

Cross-functional insights that foster critical alignment and collaboration across organizations

2023 Program Lineup

Engage and contribute in plenaries aimed at breaking barriers and solving problems, along with in-depth breakouts and the Solutions Exchange!

Sessions Include:

  • Returning to the New Normal in the Face of Evolving Challenges: Update from CDRH Director, Jeff Shuren
  • Medical Device User Fee Amendment (MDUFA) V: How Is It Impacting FDA Staff, Industry, and Patients?
  • Office of Regulatory Affairs (ORA) Office of Medical Device and Radiological Health Update
  • Finding Common Ground: Managing Device Interoperability Expectations
  • Situation in UK & Switzerland
  • Sustainability Throughout the Supply Chain: FDA and Industry Perspectives
  • FDA Transition to ISO 13485/Update on Proposed Rule Aligning QSR With 13485 (QMSR)
  • Global Regulatory Convergence and Shaping Innovation
  • Innovating Submission of Premarket Applications – CDRH Portal and eSTAR Program
  • Demonstration of FDA Databases and Publicly Available Tools

2023 Speaker Highlights

Jeff Shuren, Director of the Center for Devices and Radiological Health, FDA-CDRH

Jeff Shuren

Director of the Center for Devices and Radiological Health (CDRH), FDA

Elizabeth Miller

Assistant Commissioner for Medical Products and Tobacco Operations, FDA-ORA

Monica Wilkins

Vice President Regulatory and Quality, Abbott

Sabina Hoekstra-van den Bosch

Global Director Regulatory Strategy, TÜV SÜD Medical Health Services

Kim Trautman, Managing Director and VP, MEDIcept

Kim Trautman

Managing Director and Vice President, MEDIcept Inc.

Keisha Thomas, Associate Director for Compliance and Quality, FDA - CDRH

Keisha Thomas

Associate Director for Compliance and Quality, CDRH, FDA

Douglas Kelly

Deputy Center Director for Science Office of the Center Director, CDRH, FDA

Phil Pontikos, Investigator, Medical Device National Expert, FDA-OMDRHO-ORA

Phil Pontikos

National Expert, OMDRHOORA, FDA (Invited)

Heather Rosecrans, Executive Vice President, Medical Devices & Combination Products, Greenleaf Health Vice President Regulatory Affairs, MDMA

Heather Rosencrans

Executive Vice President, Medical Devices & Combination Products, Greenleaf Health
Vice President Regulatory AffairsMDMA

RAPS Regulatory Affairs Certificate (white)

Are you a current RAC holder? 

Attend MedCon 2023 and earn 12.0 RAC recertification credits. 

MedCon 2023 Sponsors

Because of the generosity of our sponsors, we can continue our work to improve the healthcare products industry.

Diamond Sponsor

Platinum Sponsors

Zimmer Biomet logo
Steris Logo

Gold

Olymus America Logo

Gold

Eli Lilly and Company

Silver

Boston Scientific Logo

Learn more about supporting MedCon 2023 through sponsorship by contacting Patrick Flynn at 301-770-2920, ext. 246 or pflynn@healthcareproducts.org.

This conference is co-sponsored by the Food and Drug Administration (FDA) of the U.S. Department of Health and Human Services. The contents are those of the presenters and do not necessarily represent the official views of, nor an endorsement by, FDA/HHS or the U.S. government.