Tuttlingen – The MedicalMountains continuing education year 2024 offers a total of 13 certificate courses. The gain in knowledge is accompanied by a saving in fees if you decide in good time: If you register up to four weeks before the start of the course, an early bird discount of ten percent applies.
The requirements for medical technology companies are diverse. The continuing education program at MedicalMountains GmbH is correspondingly extensive so that you can acquire the individually required modules and apply them directly in practice. But if it is also a matter of examining processes in their entirety and relating the partial aspects, certificate courses are the method of choice. For them, the following applies: A certificate course is more than the sum of individual events - a holistic understanding is more than a string of isolated findings. This know-how is indispensable in the daily activities of a medical technology company in order to be able to move efficiently and safely into the future.
There are a total of 13 certificate courses in the program for 2024. New are “Clinical Affairs Manager”, “Sustainability Manager Medical Technology” and “Technical Documentation Manager”. The “Medical Technology Quality Manager” has received a “facelift”; More fundamental QM and MDR aspects will be represented here in the future. In order to ensure the quality of knowledge transfer, the number of participants per certificate course is limited. Early registration is also advantageous from a second point of view: an early bird discount of ten percent applies up to four weeks before the start of the course.
The certificate courses in chronological order:
Quality manager for medical technology
Start: March 12, 2024
Content
Equipped for the diverse challenges in quality management: The certificate course provides participants with a comprehensive portfolio of knowledge and tools - so they can not only find out what requirements exist, but also how they can be specifically implemented in the company.
target group
Employees in quality management who are responsible for implementing the specific requirements in the development, manufacture and monitoring of medical devices and who want to bring their technical knowledge up to date, as well as managing directors or QM specialists who would like to switch to medical technology from other industries.
Regulatory Affairs Manager
Start: April 11, 2024
Content
On the one hand, regulatory affairs managers are responsible for working closely with authorities and testing bodies with regard to national and international requirements and regulations
