Keeping pace with evolving global regulations, complex product lifecycles, and new technological standards isn’t just a challenge—it’s a daily reality. Eurofins Medical Device Consulting offers a comprehensive portfolio of customised training and seminar services designed specifically for professionals working across the medical device sector. Delivered on-site, online, or through hybrid formats, our programmes are created and led by subject-matter experts with decades of hands-on regulatory and technical experience. 

We collaborate closely with your teams to understand your operational context, then build tailored learning programmes that target your exact needs, from foundational regulatory knowledge to specialist compliance strategies.

Our training offering covers a wide range of regulatory and technical topics, including:

• Quality Management – ISO 13485/QSR
• EU MDR 2017/745
• Software lifecycle management – IEC 62304
• Risk Management – ISO 14971
• Design Control Process
• Clean room qualification and management  – ISO 14644
• Sections in ISO 13485 such as: GDP, economic operators, traceability, process and product control etc.
• Biological Evaluation – ISO 10993 series
• Reprocessing