Veranstaltungen

[WEBINAR] Build compliant Technical Documentation (TD) under MDR

Did you know it takes between 6 and 18 months from application to issuance of the MDR certificate for 80% of the companies?

Did you know 50% of the submitted TD are incomplete at first?

To expedite the Technical Documentation review process by the Notified Body and avoid extra costs and delays (which potentially could make your company miss the May 2024 deadline), your technical documentation submission needs to be right the first time!

Medidee supports your MDR transition process. During this webinar, our experts Lydie Moreau and Philippe Etter will tell you all about:

– What are the additional requirements of MDR compared to previous directives
– What is the structure your TD should comply to
– How to make sure you have a clear traceability thread within your TD to demonstrate compliance to all GSPRs

Interested in joining us? Register here!

Free info session to discover CARAQA program in Muttenz on September 6th 

Progress towards your company’s decision-making centers and play a key role in maintaining your company’s competitiveness and sustainability while successfully navigating all the regulatory challenges.

Join this 6 months program to become a Clinical Affairs, Regulatory Affairs & Quality Assurance specialist for Medical Devices and IVDs.

During 1:30, David Hradetzky from FHNW and Philippe Etter from Medidee will tell you more about this CARAQA program in Muttenz, Switzerland, offered in partnership with FHNW, The University of Applied Sciences and Arts from the Northwestern Switzerland.

Next starting date is in January 2023, want to know more?

Reserve your seat now and join us on FHNW Campus on September 6th from 6 to 7:30PM CEST.

Book your seat here.

Join us live on FHNW Muttenz Campus for the next CARAQA FHNW Info session on September 6th!

Prepare yourself for the next CARAQA program which will start in January 2023!

Philippe Etter and David Hradetzky will present you the program and answer all your questions.

Be part of the next CARAQA Muttenz class and become a Clinical Affairs, Regulatory Affairs, and Quality Assurance specialist with this recognized training!

Our Certificates of Advanced Studies is sponsored by Swiss Medtech and Medidee.

Click here to book your seat for the Info session

For additional info on all our programs, visit Caraqa’s website

Contact us for any request at training@medidee.com

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