With experts attending our focus days, we offer comprehensive points of contact for Manufacturers in the homecare sector.
Are you new to the medical device market and have lots of questions about the MDR ,? We have provided you with a lot of information on the topic of "MDR and requirements for start-ups" and answers to important questions, such as
- Do I really have a Medical Device and what does that mean for me?
- What about the classification?
- How do I combine my medical device with other (medical) products?
- When is the right time to set up the CE documentation or can I do it afterwards?
- Is there more to consider besides the MDR?
- Wer entlastet mich auf dem Weg zum CE oder schaffe ich das allein?
- What happens after the CE?
- What costs can I expect?
- How long does such a conformity assessment procedure take?
- When do I contact the Notified Body?
If your question is not yet listed, please send us your request by contact and come to the "MDR and requirements for start-ups" on 16.09.2022 at our stand at REHACARE.
You will find us from 10:00-18:00 in Hall 4 Stand E03..
We look forward to your visit!
Further focus days at REHACARE:
- 14.09.2022 "Day of solution for listing issues"
- 15.09.2022 "Quality management for manufacturers of medical devices"
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