Regulatory Affairs for Medical Devices mini course

Dear ,

Are you working on innovative medical devices?

Navigating the complex regulatory landscape is crucial for getting your medical device to market, and we're here to help you master it! Our latest online course, Regulatory Affairs for Medical Devices, is designed specifically for those looking to accelerate their journey from development to commercialization.

The purpose of this course is to help you:

Understand the regulatory pathway for medical devices in the US, focusing on FDA requirements.

Learn how to classify your device and determine the correct pre-market submission pathway.

Ensure post-market compliance, including quality management, registration, listing, and ongoing safety monitoring.

Receive tailored guidance through 1:1 mentoring session, helping you tackle specific challenges with expert support.

Check here for more information!

📅 Date:

Week of 18 to 22 of November

📍 Local:

Online sessions

Should you have any questions, do not hesitate to contact me: soraia.caetano@bgi.pt!

Best regards,

Soraia Caetano, Project Manager at BGI - Sustainable Ventures

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