The Regulatory Affairs Professionals Society (RAPS) is the largest global organization of professionals involved with regulatory and quality for healthcare products, including medical devices, pharmaceuticals and biologics, diagnostics, and digital health. Founded in 1976 as a neutral, nonprofit organization, RAPS supports and elevates the regulatory profession with education and training, professional standards, publications, research, networking, career development, and other valuable resources. RAPS is home to the Regulatory Affairs Certification (RAC), the only post-academic professional credential to recognize regulatory excellence. The society is headquartered in suburban Washington, D.C., with chapters and affiliates worldwide. www.raps.org 

RAPS Euro Convergence is the most comprehensive regulatory affairs event in Europe. It focuses on the latest topics and developments in healthcare products, including medical devices, IVDs, pharmaceuticals, combination products, regulatory business, and digital health. The event unites regulatory affairs professionals and industry partners to share and collaborate on solutions for the

improvement and advancement of healthcare in Europe. www.raps.org/euroconvergence

MedBoard is the only all-in-one automation and knowledge platform for Regulatory, Clinical, Market and PMS processes in Medtech, Pharma and Life Sciences.

By uniquely combining comprehensive Global Databases, Software Products, and AI solutions, MedBoard is transforming how professionals and teams access knowledge and increase processes productivity, empowering them to know more and do faster (www.medboard.com).

V-Apps specializes in providing eQMS solutions for pharmaceutical and medical device companies. Their cloud-based QHSE (Quality, Health, Safety & Environment) platform helps organizations streamline regulatory compliance and operational processes.
With AI-powered insights, predictive analytics, and customizable workflows, their approach makes them a trusted partner for organizations navigating complex regulatory and operational challenges. (www.V-Apps.cloud).

TraceX is a free, AI-powered platform designed to manage the entire product lifecycle from design to market launch and beyond with full regulatory compliance.

Whether targeting CE, FDA, or ISO standards, TraceX ensures your team is always audit-ready. An all-in-one solution for quality processes, technical documentation, and compliance management fully integrated, open-source, and free. Built for regulated industries like medical devices, pharma, and biotech. From consultants and startups to established companies, TraceX is built for you. (www.tracex.co).

My Audit Corner is the AI assistant for Quality and Regulatory Affairs (QA/RA) teams in the medical device industry. Our platform turns ISO 13485 audit prep and MDR technical documentation into a controlled workflow: automated gap analysis, consolidated technical files, CAPA traceability, evidence generation and regulatory watch. Built by and for QA/RA professionals, the tool speaks your language (notified body, MDD-to-MDR transition, post-market surveillance) and plugs into your existing QMS in a matter of days. Less time on paperwork, more peace of mind on audit day. (https://myauditcorner.com/en/).

Founded in 2002, the European Association of Authorised Representatives (EAAR) represents Authorised Representatives operating under EU medical device legislation and works to strengthen professional conduct, competence, and understanding of AR responsibilities under the MDR and IVDR. As the flagship expression of this mission, the EAAR MDR/IVDR Summit 2026 will take place on 8–9 September 2026 in Brussels, Belgium, marking its 10th edition. The Summit brings together Manufacturers, Authorised Representatives, Notified Bodies, Competent Authorities, and Regulatory, Quality, and Compliance professionals to discuss the practical implementation of the evolving MDR and IVDR landscape. The programme focuses on key topics including regulatory enforcement, EUDAMED, clinical evidence, post-market surveillance, vigilance, AI and the evolving responsibilities of economic operators. Through expert-led sessions, panel discussions, and networking opportunities, the Summit provides a platform for sharing practical insights, fostering collaboration, and supporting the MedTech community in navigating Europe’s evolving regulatory landscape. (www.eaarmed.org).