
Medical Device HQ
In-house training, public and online courses on managing and developing safe medical devices
Recent posts
- The illustrated guide to quality management for medical devices and ISO 13485
- Education and training requirements for the PRRC under the MDR: Meeting auditors’ expectations
- Design risk assessment, process risk assessment, and use risk assessment for medical devices – the danger of division (Part 3)
- Design risk assessment, process risk assessment, and use risk assessment for medical devices – the danger of division (Part 2)
- Design risk assessment, process risk assessment, and use risk assessment for medical devices – the danger of division (Part 1)
Categories
Would you like to learn more about risk management or design control?
Take a look at our online Risk Management course on ISO 14971:2019 and online Design Control for Medical Devices course.
These courses are taken by both competent authorities, notified bodies and medical device manufacturers and distributors.