Welcome to
- your regulatory partner
The two regulations include stricter clinical requirements for manufacturers to obtain a new CE marking and for maintaining access of their healthcare products for patients and users within the EU/EEA
If your organization is
- a medical device Notified Body with MDR/MDD active device clients looking for a Senior Clinical Expert for your clinical evaluation assessments
- a Notified Body looking for a theoretical and hands-on training program for your MDR clinical experts/clinicians
- a regulatory consultancy partner providing support to manufacturers concerning clinical data, device equivalence and clinical investigations, to confirm clinical safety, performance and patient benefit of its active medical devices
- a medical device manufacturer or other stakeholder seeking clinical competence to review and/or approve your clinical evaluation documentation
We assist you in a timely manner through the above processes
About
has extensive experience from assessment of MDR/MDD documentation and conformity procedures. Our primary consultant focus is on the key elements of clinical evaluation and post-market monitoring, covering intended use, risk analysis, CEP and CER, as well as post-market plans and PSUR. We also assist in the clinical documentation review and approval to fulfill the manufacturer´s clinical competence requirements
At we have the unique competence combination of engineering, clinical healthcare (MD) and clinical research (PhD) in addition to extensive experience from the international medical device industry
We would like to point out that impartiality and conflict of interest are important to us and which we carefully evaluate in our consulting agreements and activities
Welcome to contact today for advisor assistance, mentorship and guidance on your clinically related regulatory processes
Contact
- MEDOTEC AB
- Email: [email protected]