Qserve MedTech Conference 2023

Venue: Novotel Amsterdam Schiphol Airport, Amsterdam, The Netherlands

Start: Wednesday 11 Oct 2023 09:00

End: Friday 13 Oct 2023 17:00

Join the 5th Qserve MedTech Conference, an exclusive program developed by Qserve Experts sharing 25 years of knowledge based on market trends. All industry hot topics will be addressed during this 3-day event. 

Everybody working in the MedTech industry and wanting to extend their regulatory knowledge will profit from the various programs and easily connect with global experts from the field.

Qserve created a special IVD stream in the conference program with topics for advanced regulatory and clinical experts as well as for starters who need to know the IVD regulations.

Day 1 will focus in the morning on the general IVD regulations – secrets to getting it right first time, where Sue Spencer (Qserve), Tom Patten (NSAI) and Colleen Watson (Thermo Fisher) are the presenters. And in the afternoon; IVDR - Lessons Learned and Challenges to Come, where Steve Lee from ABHI, Tom Patten (NSAI) will co-present the session with Sue Spencer.

The latest hot regulatory issues and challenges will be discussed by a panel of (industry) experts, and Steve Lee will co-present the session about the UKCA Strategy. 

In the afternoon, you can join to participate in the panel discussion by asking your questions to the experts.  

Day 2 will be focused on hot issues outside of the EU and a dedicated presentation on IVD Go-to-Market strategies to focus on the FDA presented by Lorry Weaver (Qserve) and Colleen Watson (Thermo Fisher).
If you are working on companion diagnostics, the session Companion Diagnostics Challenges for Pharma and Diagnostic Partners to Work Together will be of special interest, presented by Jude O’Donnell (Qserve) and Maria Orr (Astra Zeneca) + João Martins (Abbott).

Day 3 is a complete training day, which can be booked as part of the full conference program or as separate participation. Qserve selected the following two topics for IVD;

  1. Training IVD focused on market access EU | Clinical evidence and clinical studies to support EU IVDR submissions (Sue Spencer, Kristiane Schmidt, and Jude O’Donnell, Qserve).
  2. Training IVD focused on market access US | FDA pre-submissions (Lorry Weaver and Jude O’Donnell).

Besides the program for IVD, there is a medical device, clinical, and global registration stream, and plenty of time for networking. You will find many peers from the industry, regulators, distributors, and Qserve. Join us for insightful keynotes, panel discussions, and workshops led by industry experts on innovation, market access, dealing with regulatory hurdles, and general growth in the health tech industry.

We will host daily panel shows, in which the speakers will address all the questions from the audience, providing a unique opportunity to approach the experts.

Highlights of the Conference:

  • Parallel tracks for medical devices and in vitro diagnostic manufacturers
  • Focus on market access in Europe & United States
  • Extra focus on clinical subjects like clinical studies, clinical evaluation, and PMCF 
  • 40+ expert speakers from Qserve, the industry, and Notified Bodies
  • Festive dinner and networking party 
  • Interactive in-depth training day 

For more information, and to register, click here.

We provide a special deal of 15% discount for ABHI members, use the promotional discount code: ABHI15, valid until 20 September.