Your Central Knowledge Hub For MedTech Regulation, Strategy And Compliance
Industry Leading Events, Webinars, Reports And Expert Perspectives To Help You Overcome Your Regulatory And Strategic Challenges
EU MDR. UKCA. EU IVDR. Global Market Regulations. Software. AI. Post Market Surveillance. Vigilance. Clinical Evaluations. Clinical Investigations. EU Medical Device Law. Compliance. Drug Device Combination Products. Biocompatibility.

The Future of MedTech Awaits: 2026 Summit Coming Soon!
The MedTech Summit 2025 may have concluded, but the journey toward regulatory excellence continues! We hope you left equipped with actionable insights, expert guidance, and valuable connections to navigate the evolving landscape of EU MDR and IVDR.
Get ready—2026 is set to be the ultimate gathering for MedTech leaders, featuring cutting-edge strategies, best practices, and unparalleled opportunities to stay compliant and competitive. Don’t miss your chance to accelerate your regulatory success. Sign up now for exclusive updates and early access to registration!
MedTech Series: Regulatory Affairs in Latin America for Medical Devices
This course is designed for regulatory professionals looking to enhance their skills in managing operations in Latin America. You will learn strategies to streamline approval processes, avoid costly rejections, and stay informed about regulatory changes in the region.
Dates for the 2026 course are yet to be announced, but you can express your interest today, and we will notify you as soon as registration opens.

Speaker Opportunities
Are you ready to take the stage and share your expertise with an eager audience? We want to hear from you!
This is your chance to shine: Submit your speaker proposal to Kaitlin Dailey at kaitlin.dailey@informa.com and be part of our upcoming events.
Let your voice and vision inspire others.