Thursday, June 17, 10:00 am - 1:00 pm ET

Tap into the power of the Regulatory Medtech community at our virtual meeting.

Join the MedTech Regulatory Community Meeting to connect with peers and industry experts to learn and share best practices to modernize regulatory. You'll hear customer use cases from experts leading digital transformation, get a product roadmap update, engage in live Q&A, and have the opportunity to join roundtable discussions.

You'll walk away with actionable insights to enhance regulatory operations and processes that will help improve speed to market, compliance, and innovation.

Agenda (ET times):

10:00 am - 10:30 am Keynote: Modernizing Regulatory Operations to Ensure Global Compliance & Speed to Market, Bausch Health

10:30 am - 11:15 am Panel: Baxter Health, Roche Diagnostics, USDM Life Sciences

11:25 am - 12:25 pm Vault RIM Product Roadmap & Q&A

12:30 pm -  1:00 pm  Roundtable Discussions

If you are not able to attend the full event you can still register to attend a portion of the meeting.

Donielle Johnson

Executive Director, Global Head Regulatory Affairs, Medical Devices

Bausch Health

Donielle leads the creation of a global medical device organization that supports strategic priorities to ensure access to innovative technology and compliance. Prior to her current role, Donielle held several global regulatory roles at Johnson & Johnson, Philips, Abbott Vascular, and Medtronic.

Jay Crowley

Vice President, Medical Device Solutions & Services

USDM Life Sciences

Prior to USDM, Jay was Senior Advisor for Patient Safety in FDA's Center for Devices & Radiological Health. He held a variety of positions during his 27 years at the FDA, including primary responsibility for development and implementation of FDA's UDI System, GHTF, and IMDRF UDI guidance documents.

Larry Litle

Senior Director, Global Strategy & Delivery

Baxter Healthcare

Larry leads Baxter Healthcare's Global Regulatory Affairs and Global Strategy & Delivery organization, with a primary focus on simplifying regulatory processes and providing strategic support to enable efficiency and effectiveness on a global scale.

Roxane Bonner

QA/RA Program Director

Roche Diagnostics

Roxane is responsible for program management, change management, and implementation for IT solutions used by QA and RA functions at Roche.

Register Now

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