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Mini course: Clinical Evaluation under MDR (free)

Would you like to know what a Clinical Evaluation for medical devices is?

Are you a Regulatory Affairs Manager and want an up-to-date overview of Clinical Evaluation requirements?

Do you want to change or develop your career in the field of medical writing for medical devices?

 

...Then this mini course is a good start!

 

You will get all the basic information on Clinical Evaluation requirements in the medical device approval process. You will learn which regulatory requirements and standards are relevant for the preparation of the Clinical Evaluation. By describing the basic processes of Clinical Evaluation, you will get an insight into how Clinical Evaluation works. In addition, you will get an overview of the required documents and related documents including PMCF & PMS plans.

The mini-course is part of the certificate course "Clinical Affairs for Medical Devices". Learn more here.

To register for free, click here.
 

If you need further guidance or would like some of these documents prepared for you, book a free initial consultation with MEC-ABC here.

 

If you would like to learn more about the MEC-ACADEMY, please visit us at www.mec-academy.de

 

We would be happy if you share your certificate on social media (Linkedin, XING, Instagram)!
 

Nadine Leistner and the MEC-Academy team

 


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