הנושאים שמעניינים אותי
(אפשר לבחור מספר נושאים)
The aim of this course is to inform the participants about the impact of the new European Medical Device Regulation that has entered into force per May 26, 2017. During the training, the new requirements will be discussed in detail and where possible will provide answers on how to implement the changes.
The...המשך קריאה
Day 1:
Day 2:
This course will be extremely useful for the persons working in regulatory and quality assurance departments, and equally important for project managers or CTO’s involved in development of new medical devices. Last but not least, as CEO of a medical device company, you will obtain a clear insight in the new EU requirements and the impact it will have on your business case or company.
At the end of the seminar, you will be able to draft your company’s action plan, enabling working towards EU MDR compliance throughout the lifecycle of a medical device.
הנושאים שמעניינים אותי
(אפשר לבחור מספר נושאים)