January 1st 2020 is the day. Then the National Implant Register (Landelijk Implantaten Register or LIR) expects a complete data file for every implant in the Netherlands. And from May 26, 2020, the rules of the Medical Device Regulation take effect.
These radical changes demand a lot of adjustments from organizations, whereby working with data from GDSN and with GS1 standards is very important. We are happy to guide you in the world of data processing and data validation.
Watch this webinar and discover:
- How to comply with the MDR legislation
- How to receive data from the GS1 datapool
- How to keep your data clean and automize your data processes so to keep the administrative tasks to a minimum
View this webinar now and avoid encountering any unpleasant surprises in the future.
