You ask. Our experts answer.
Accumulated knowledge in the field of medical devices and in vitro diagnostic medical devices along with informative one2one discussions with our experts - all this is waiting for you in November 2020. We have prepared a whole series of new webinars on the topics of MDR, IVDR and testing, and will present them to you on three consecutive days. Be excited about a knowledge-sharing event packed with information by professionals for professionals.
In addition to our 12 webinars, you can now also book one2one expert talks where you get your questions about about MDR, testing and IVDR answered by our specialists.
We look forward to your registrations for both the webinar series and the expert conversation. Take advantage of this opportunity and benefit from our comprehensive knowledge!
Our webinar series will take place from 3 to 5 November 2020. Each of day will contain around four online presentations, held once in the morning from 8:30 am CET and once in the afternoon from 4:30 pm CET. This provides you with optimal flexibility in planning your participation
3 November: Testing
The first day of our webinar series will focus on the topic of medical device testing. Our specialists will turn you into professionals in the field of cyber security and biocompatibility testing. We will also take a look at the safety and essential performance standards of medical electrical equipment and provide you with comprehensive information on electromagnetic compatibility and the special requirements for medical devices with wireless functionality.
8:30 am CET and 4:30 pm CET | Francisco Navarro: Cybersecurity for medical devices
9:30 am CET and 5:30 pm CET | Dr. Christian D. Lindner: Medical device testing for biocompatibility – MDD and MDR requirements
10:30 am CET and 6:30 pm CET | Dr. Tobias Beck: Testing in accordance with the IEC 60601-1 series for Active Medical Devices
11:30 am CET and 7:30 pm CET | Hannes Adelsberger: Medical device testing for EMC/radio compliance – Requirements of MDR and RED
Day two of our series is dedicated to the current medical device regulation. The Medical Device Regulation, or MDR, presents manufacturers with quite an extensive catalogue of requirements. We bring light into the darkness of the MDR and the specified requirements.
8:30 am CET and 4:30 pm CET | Martin Witte: Technical Documentation under MDR
9:30 am CET and 5:30 pm CET | Robert Madjno: Understanding Clinical Data under the MDR
10:30 am CET and 6:30 pm CET | Dr. Julia Hoyer: MDR lessons learnt
11:30 am CET and 7:30 pm CET | Dr. Sabine Hoekstra: MDR additional authority consultation procedures
5 November: IVDR
On the last day of our webinar series, the In Vitro Diagnostic Regulation (IVDR) is on the agenda. Which standards have to be met by manufacturers? What needs to be considered when creating technical documentation? How does testing work? We will clarify these and many other relevant issues connected with IVDR.
8:30 am CET and 4:30 pm CET | Marta Carnielli: Technical Documentation under the IVDR
9:30 am CET and 5:30 pm CET | Dr. Thomas Theisen: Clinical evidence in IVDR Technical Documentation
10:30 am CET and 6:30 pm CET | Dr. Alexander Stock and Martin Heinrich: IVD Equipment Testing: Software & Electrical Safety
11:30 am CET and 7:30 pm CET | Marta Carnielli: IVD classification under the IVDR
This is an individual conversation by professionals for professionals. The specialists from our medical device webinars are also available for detailed one2one discussions. During these sessions, they will exclusively address your individual questions. Benefit from their comprehensive experience and expert know-how and book your one2one conversation now.
Three easy steps to your individual conversation
Select Your Location
Bosnia and Herzegovina