Risk Management for Medical Devices ISO 14971
Supplementary training is often overlooked by medical device professionals until it is triggered by an upcoming Notified Body and/or ISO 13485 certification audit. Our experts all have many years of “real” experience in their own particular areas of the Medical Device
Industry, ensuring your company a high-quality training session.
Who should attend?
- Senior Management
- Quality Managers and Regulatory Affairs
- Product Developers and Product Managers
- Members of Risk management teams
- Anyone involved with the implementation of
Medical Devices to the market
The number of participants is maximized to nine to provide a stimulating and practical working environment.
We offer open enrolment, on-location, train-the-trainer formats.
Please contact us to schedule in-house training, which is also recommended for training multiple colleagues or teams at the same time.