Stay up to date as a Medical Device Advisor
Welcome to our high-quality e-learning program for medical device advisors in accordance with Section 83 MPDG.
As a medical device advisor, you are responsible for regularly refreshing your expertise. Our refresher e-learning program helps you to continuously update your knowledge of regulatory requirements, legal principles, and the most important tasks of your role. Of course, we also take into account the current version of the Medical Devices Operator Ordinance (MPBetreibV) so that you always remain up to date with the latest regulatory requirements.
Whether as a refresher after your basic training or to deepen your knowledge, this course ensures that you are always up to date with the latest requirements and can perform your work professionally and in compliance with the law.
Why should you choose our refresher eLearning course?
- Industry-specific expertise: Our course has been developed by experienced medical device professionals to ensure that you acquire practical knowledge.
- Flexible eLearning: Learn at your own pace and in a place of your choice. Our eLearning approach allows you to optimize your schedule while still receiving high-quality training content.
- Interactive modules: Boring theory is a thing of the past! Our interactive modules teach you in an engaging and practical way. From case studies to quizzes, you will be actively involved in the learning process.
- Certificate for your career: Upon successful completion of the MDA Refresher eLearning course, you will receive a certificate confirming your qualification as a medical device advisor.
- Content
- Update on the legal requirements of medical device law in Europe and Germany
- Refresher on the tasks, duties, and responsibilities of a medical device advisor according to § 83 MPDG
- New developments in medical device monitoring and reporting requirements
- New developments in the Medical Device Operator Ordinance (MPBetreibV)
- Differences from the person responsible for regulatory compliance (MDR Article 15)
Note on your personal learning environment:
After registering, you will receive access to our LMS platform so that you can view the course flexibly at any time. After completing the e-learning course, you will receive a certificate of qualification. - How you benefit
- You will always stay informed about regulatory changes and current requirements.
- You will be able to communicate with customers, users, and authorities in a legally compliant manner.
- You will regularly receive a certificate as proof of your current expertise in medical device consulting.
- Flexible time management: You have 180 days to complete the e-learning course at your own pace – ideal for combining learning with your everyday working life.
- Methods
Trainer input, tasks, practical cases, storytelling.
- Target Audience
- Medical device consultants
- Medical device sales staff
- Customer service and technical support staff
- Quality management and regulatory affairs staff
- Healthcare professionals who sell or support medical devices
