The new regulation on medical products has entered into force as from 2017. All manufacturers of medical products must familiarize themselves with the new requirements. The regulation has far-reaching implications and affects all classes of medical products.
Among the aspects changed are the classification of products, previous basic requirements, technical documentation, clinical evidence, market surveillance, and quality management systems. The new scrutiny procedure, reprocessing requirements, and the introduction of the European database Eudamed also bring about profound changes. In our seminar, you will gain a compact overview to align your company with the new requirements of the Medical Device Regulation (MDR).
The British Academy for Training and Development offers this course to the following categories:
After completing the program, participants will be able to master the following topics:
Note / Price varies according to the selected city
Maintenance of Medical Devices and Identification of Faults
2024-10-07
2025-01-06
2025-04-07
2025-07-07