Regulatory & Clinical Checkup
Register now for a free checkup with the experts of Medidee, our satellite event partner.
The event will be online. It is dedicated to Medtech companies (MD and IVD) that may have questions related to the classification of their medical device / IVD or that are questioning the classification of their products as medical devices, the conformity assessment route or the requirements in terms of clinical evidence.
Example of topics that might be covered:
- Classification strategy (under MDD/IVDD and MDR/IVDR) of a complex systems, borderline products
- Clinical evaluation requirements of innovative IVD devices
- Conformity assessment route and the context of Covid-19 crisis
- Evaluating your regulatory positioning
- Evaluating the impact of new European regulations (MDR & IVDR) on your strategy
- Confirming or building a safe plan including quality and clinical aspects.
Any question? Please send an email to Silvia Anghel from Medidee.
If you wish to book your seat for a 1-hour free discussion, please let us know the following points:
- Your preferred time slot (2 options): 09:00 / 10:15 / 11:30 / 12:45 / 14:00 / 15:15 / 16:30
- Company name and website
- Product type (IVD / MD)
- Questions related to Quality / Regulatory / Clinical
- Name of the participants