Join QbD at the MedTech Summit 2023
8 Cutting-Edge Topic Streams Covering EU MDR/IVDR, Clinical Investigations, Post-Market Surveillance, Software/AI, Biocompatibility, Law & Compliance, and Global Market Access
Critical Insights from EU Commission, Competent Authority, Notified Body, and Medical Device and IVD Industry Pioneers
Schedule a meeting with our experts
The QbD Group provides expertise in quality assurance, validation, regulatory affairs, clinical, quality control, software solutions, and go-to-market strategies for companies in the biotech, small molecules, digital health, medical device, and IVD industries.
We are available to assist you during the MedTech Summit 2023. Schedule an appointment below if you’re interested in our services.