CMS SciDoc invites Expressions of Interest for our Medical Device Training Programmes – 2026, designed to empower professionals with practical expertise and up-to-date insights into global regulatory requirements.
Our programs are crafted and delivered by experienced medical device consultants, blending regulatory theory with real-world, hands-on application to help you achieve compliance confidence.

Who should attend?
💠 Regulatory Affairs & Quality professionals
💠 Medical device manufacturers & sponsors
💠 Start-ups entering the medical device market
💠 R&D, Clinical, QA/RA, and Compliance teams

Proposed training topics:
💠 ISO 13485 – Quality Management Systems for Medical Devices
💠 ISO 14971 – Risk Management for Medical Devices
💠 Process Validation for Medical Devices
💠 Medical Device Software
💠 Auditor Training
💠 Designing a Regulatory Compliant Technical File
💠 Clinical Evaluation Report: Tips & Tricks
💠 MDSAP Training
💠 MDR Training

Ready to get ahead in 2026?

Register your interest today by contacting info@cmsscidoc.com.

Spaces are limited to ensure interactive and high-quality learning — secure your place early and take the first step toward regulatory excellence this year!