Date
Post Date
july, 2021
Event Details
This training provides you with the basics of regulatory affairs in MedTech with a focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical
Event Details
This training provides you with the basics of regulatory affairs in MedTech with a focus on MDR and IVDR (Medical Devices and In-Vitro Diagnostic Medical Devices Regulation).
Get an overview of the regulatory landscape, hear about the basic concepts and principles and get insights into the necessary steps but also pitfalls when bringing a MedTech product to the market.
Discuss with Medidee experts about the different Steps to CE marking for Medical Devices; US Market Access for MD and V&V and Technical documentation!
Ready to participate? Register now, it’s free of charge!
Time
June 29 (Tuesday) 10:00 am - July 1 (Thursday) 12:00 pm CEST
Location
Online Event
Event Details
If you are a Germany-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices and in vitro diagnostics), this event is for you! Together
Event Details
If you are a Germany-based company with questions induced by the new MDR (classification, clinical testing & quality management of medical devices and in vitro diagnostics), this event is for you!
Together with our partners, we offer you an exclusive free check of your situation with regard to the new regulatory requirements.
During 1 hour, our Medidee experts will answer your questions and will guide you to the next steps!
Find out more and sign up for free 👉 here
⚠️ Hurry, slots go fast! First come, first served ⚠️
Medidee – Compliance with Relevance
Time
(Tuesday) 9:00 am - 4:00 pm CEST
Location
Online Event