The EU Medical Devices Assistant on the GPT Store
GPT Description
GPT Prompt Starters
- Explain the Annex XVI requirements under EU MDR.
- How do I classify a medical device under the new EU MDR?
- Detail the post-market surveillance obligations for Class IIa devices.
- What are the key differences between MDD and MDR for medical software?
The EU Medical Devices Assistant GPT FAQs
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