Key Regulatory Insights for US & EU Medical Device Market Access

		Location	Price
Online	Online		Book

Did you know...

Approval in one jurisdiction has often been unofficially acknowledged as an indication of a device’s quality, facilitating approval in another?

The importance of entering the US or EU markets with success heavily influences your probability of excellent market penetration in the other. To succeed, you need:

• Robust planning to manage changes in regulations and personnel

• Ensure transfer knowledge into your team

• Clinical trials that represents the patient population in each jurisdiction

• Patent protection and local representation

DQS and RegDesk are ready to guide you in a free online seminar.

Join the Director of North America's Medical Business at DQS, Yuan Li and our partner RegDesk's Jodi Granger, Director of Regulatory Affairs, to understand the differences, similarities, and key opportunities for expansion into the US and EU markets in 2025.

woman sits on the couch with a laptop and a headset taking notes on a notepad during a workshop

DQS and RegDesk bring you 2024 regulatory insights for the Medical Device market

Similarities and Differences: US and EU Market Access

What Will You Learn in This Webinar?

Key similarities and differences between the regulations in the US and EU markets for medical devices, and strategic approaches to navigate your regulatory pathway.

Gain insights to enhance your:

• Global Framework for Regulation of Medical Devices

• Device design

• Development process

• Supplier selection

• Clinical trials

• Regulatory pathways

…to obtain successful approval and market entry of your medical device.

About Jodi Granger, Director of Regulatory Affairs at RegDesk

Jodi brings over 35 years of experience in quality and regulatory roles within the medical device and IVD industry. She has held leadership roles, overseeing global regulatory teams and driving the development and execution of regulatory strategies for all classes of medical devices worldwide.

With a strong background in project management, Jodi has a proven track record of streamlining regulatory processes to enhance efficiency and ensure compliance.

Save your seat, today: