Sharing request | Regulatory Affairs for Medical Devices

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Dear ,

I hope this message finds you well!

We are excited to announce the launch of our Regulatory Affairs for Medical Devices course, designed specifically for health tech startups and research groups aiming to navigate FDA regulations and bring their devices to market.

We’d greatly appreciate your help in sharing this course with your network. To make it easy, we’ve created a dissemination kit with images and text suggestions.

Thank you in advance for your supporting this initiative.

Let us know if you need any additional information or materials!

Best regards,

BGI Team


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:

1.

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

2.

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

3.

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

4.

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

Check here for more information!
Packs

📅 Date:

January 29th to 31st 2025

📍 Local:

Online sessions

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

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