Courses and Consultancy
Get up to speed with the latest medical device standards and regulations.
Browse the courses and consultancy we can offer you at your location.
Available to medtech companies throughout the EU.
2020
The NEW MDR Medical Device Regulations
The new rules are covered in two days of intensive training covering the entire MDR and some MDD. Tailored to your product group.
Add a day of consultancy for support and implementation.
2020
Usability Engineering EN62366-1
A popular course for companies taking a user centric approach to design and development. Tailored to your product group.
Add a day of consultancy for support and implementation.
2020
Biocompatibility - A Risk Based Approach
A thorough 1 day course on biocompatibility assessments, risk based plans etc.
Add a day or two of consultancy for additional support and implementation.
2020
Software & Apps
Is your app a medical device? Ensure your software and apps meet the latest FDA & EU requirements with this in-depth 1 day course.
Add a day or two of consultancy for additional support and implementation.
2020
Quality Management for Medical Devices & ISO 13485
A course that is relevant for anyone working in medical device development.
Add a day of consultancy for additional support and implementation.
2020
Risk Management for Medical Devices & ISO 14971
The 2 day course will give you the knowledge to complete a medical device risk management file and more.
2020
Unique Device Identification UDI
A popular course for companies taking a user centric approach to design and development. Tailored to your product group.
Add a day of consultancy for additional support and implementation.
2020
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