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FDA Strategy & Regulatory Practice Event for Medical Device Companies | Free Expert Session


Join Us for an Exclusive FDA-Focused Event for the Medical Device Community

NAMSA, together with Virtonomy GmbH, Paconsult GmbH, and Kalms Consulting GmbH, is pleased to invite medical device professionals to a free, in-person, 3-hour expert session dedicated to FDA strategy and regulatory practice.

The event will be led by Dr. Adam Saltman, a NAMSA expert and former Medical Officer at the U.S. FDA with more than 12 years of hands-on regulatory experience. The session is designed to be practical and interactive, focusing on real challenges faced by medical device companies today.

Participants will gain clear, actionable insights into how to work effectively with the FDA, supported by real-world examples and open discussion.

What the Session Will Cover:

  • How to manage increasing regulatory expectations with limited internal resources
  • Practical guidance on what works, and what to avoid, when engaging with the FDA
  • An outlook on where FDA regulation is heading
  • Case studies from real regulatory projects
  • An interactive Q&A with a former FDA Medical Officer Dr. Adam Saltman

A networking lunch, kindly sponsored by NAMSA, will provide additional time for informal exchange with peers.

Event Details:

Places are limited. We encourage you to register early.

Register for FDA Focused Event here!

We would be pleased to welcome you in Munich, Ochsenhausen, or Berlin in our office, to spend the afternoon exchanging perspectives on current FDA challenges and practical regulatory approaches.

We look forward to welcoming you in person!

For more information, please contact us at info@kalmsconsulting.com or visit the NAMSA event page here.

The image utilized in this article was sourced from unsplash.com in accordance with the license terms of use.

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