Meet the Experts Netherlands: The Journey to Market Readiness

What is the event about?

Navigating MDR and QMS certification journey can be complex: from initial application and conformity assessment through to post-market surveillance. 

This event brings you face to face with BSI's regulatory experts and technical specialists, sharing their knowledge of what good submissions look like, how to avoid common pitfalls, and how to stay ahead of evolving requirements. You'll hear the latest updates on MDR and QMS and other topics shaping the industry. 

Beyond the programme, you'll have the opportunity to connect with your peers across the MedTech community, asking questions, exchanging experiences, and building valuable networks. 

Whether you're bringing your first device to market or managing an expanding portfolio, this event gives you the knowledge and connections to move forward with confidence.

Why Attend?

  • Information about the latest MDR updates, including current timelines and regulatory requirements; 
  • Insight into what makes a strong submission, and how to avoid common pitfalls; 
  • Clarity on the conformity assessment process, from application through to post-certification; 
  • Best practice guidelines on planning timelines and preparing documentation; 
  • FAQs sessions with BSI regulatory experts; and 
  • Networking with BSI assessors, technical specialists, and MedTech peers.

Who Should Attend?

Whether you're starting the certification process, looking to transfer or need to discuss your options, we can guide you through the process.

Regulatory Affairs (RA) and Quality Assurance (QA) professionals involved in submissions and compliance;

R&D teams designing products with regulatory requirements in mind;

 


Startups
navigating MedTech certification for the first time;

SMEs strengthening their regulatory readiness and Established manufacturers seeking clarity on evolving requirements.

You can book a 1-to-1 meeting with a representative of our team.

Up to 2 participants per company will be admitted to the event to allow diversified companies to participate and engage.

Event Video

  • Insightful Presentations – BSI’s Industry leaders and regulatory experts share insights on navigating MedTech compliance.
  • Interactive Sessions – Direct engagement with regulators to clarify expectations and address compliance concerns.
  • Network with Industry Peers – Connect with like-minded startups and key stakeholders in the HealthTech ecosystem.

Event Details

WHEN

25 November 2026
09:00-16:15 CET

WHERE

Van der Valk Hotel Schiphol

3 A4
Hoofddorp, NL-NH 2132 MA
Netherlands

PLANNER

BSI Medical Devices