Navigate MedTech Compliance with Expert Guidance

The MedTech industry is filled with complex regulatory challenges — but startups don’t have to navigate them alone. Join us on March 27 at Thayer School of Engineering to gain the insights and strategies needed to bring your innovations to market.

What You’ll Gain:

We’ve brought together top MedTech experts and industry leaders to help startups successfully navigate the regulatory landscape — from securing FDA approvals to maintaining post-market compliance. Here’s what you’ll gain:

 Expert Knowledge – Hear directly from professionals who have guided medical device innovations through FDA approvals, EU MDR compliance, and quality management systems.
 Actionable Strategies – Learn practical approaches to streamline regulatory pathways, mitigate compliance risks, and avoid costly delays at every stage of development.
 Meaningful Connections – Engage with MedTech founders, regulatory specialists, and industry leaders in an intimate setting designed for knowledge sharing and collaboration.

Join us to sharpen your regulatory expertise and build relationships that can accelerate your MedTech journey!

 Spots are limited. Register now!

Looking forward to seeing you there!

— The MedTech Collaborative Team

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