Clinical Evaluation has become one of the most critical — and challenging — domains under the EU MDR. But how does one build real expertise in this field?
In this episode of the Medical Device Made Easy podcast, Monir El Azzouzi interviews Florian Tolkmitt, Clinical Evaluation Expert at Pro-Liance, to explore his journey from engineering into clinical evaluation and regulatory science.
The discussion covers:
- Florian’s education and early career path
- How he specialized in Clinical Evaluation
- Key lessons learned since the implementation of the EU MDR
- What Notified Bodies really expect from clinical documentation
- Frequent mistakes manufacturers make in clinical submissions
- The evolving role of consultants in supporting compliance
- How AI and digital tools may transform literature review and evidence generation
- Advice for young professionals entering the MedTech field
This episode offers practical insights, career inspiration, and forward-looking perspectives for anyone working — or aspiring to work — in clinical evaluation and regulatory affairs.
Who is Monir El Azzouzi?
Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies, particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people better understand Medical Device Regulations worldwide. He has now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through videos, podcasts, online courses… His company also acts as Authorized Representative for the EU, UK, and Switzerland. Easy Medical Device becomes a one-stop shop for medical device manufacturers that need support on Quality and Regulatory Affairs.
Links
Linkedin florian: https://www.linkedin.com/in/florian-tolkmitt-clinical-evaluation/
Social Media to follow
The post From Engineer to Clinical Evaluation Expert – The Journey of Florian Tolkmitt appeared first on Medical Device made Easy Podcast. hamza benafqir |