MDR Compliance – Key Lessons from a Medical Product Launch

NXTGEN Hightech Biomedical and High Tech NL cordially invite you to an inspiring webinar on October 17, 2024, from 16:00 to 17:00 CET.

In this interactive webinar, Henk Stapert, CTO at smartQare, will share his extensive experience in the development and market introduction of viQtor, an innovative remote patient monitoring solution. The viQtor received its MDR approval at the end of 2022, and Henk will take you through the journey from concept to market launch and beyond, with a special focus on MDR compliance. This process continues throughout the entire product lifecycle. The connection with IVDR regulations will also be discussed, supported by practical examples. In addition to valuable insights, the webinar will provide an opportunity for interactive discussions to deepen your understanding of the complex medical regulatory landscape.

What to expect:

You will gain insights into:

• The crucial importance of early regulatory involvement.
• The key milestones for a successful product launch and how to avoid major consequences from potential mistakes.

Who should attend?

This webinar is intended for professionals in Bio- and Medical Technology and Life Sciences who wish to successfully navigate the complex regulatory landscape and bring their innovations to market faster and more effectively.

Note: There are only a limited number of spots available. Register early to secure your participation!

Do you have any questions in advance? Send them to lifesciences@hightechnl.nl. We will address them during the webinar or afterwards.

Don’t miss this unique opportunity to enhance your knowledge of regulatory requirements and accelerate your path to market success.

Register here