Vigilance and Post-Market Surveillance definition, differences and their scope. Visit our webpage for all the details!
Authorised representative (AR)
EU Parliament vote on the proposal for a revised Radio Equipment Directive passes: One step closer to a common charging solution for all?
One more step is taken towards a common charger in the EU for all electronic devices. Learn more!
General Product Safety: updating the 2020 industrial strategy for a stronger single market
On June 30, 2021, the Commission published the draft for a new GSPD. Read all the detail in our article!
EU IVDR now applies in Europe:What should IVD manufacturers do to comply?
If you are unsure of how you should now proceed in order to import new devices or maintain the previous ones in the European territory, this webinar is what you were looking for! Register now!
Compliance Success Stories: Meet Samsara Vision!
An interview with Samsara Vision about the different compliance steps and the process to launch their products in the market.
What is the Common list of COVID-19 rapid antigen tests?
Rapid antigen tests are widely used in the European Union and are helping to strengthen many countries testing capacities. For more information visit our page!
Toys containing aqueous media: New Revision of Protocol on Microbiological Safety
This protocol provides a specification of the microbiological requirements on toys covered by its scope and since there are no particular microbiological requirements for toys, the Notified Body toys group elaborated a protocol on the basis of the requirements for cosmetic products. Read more..
Marine Equipment Directive: Market Surveillance discussions
In November 2021, ADCO MED published an information document on Directive 2019/90/EU. The document collects answers on various topics discussed by the Member States market surveillance authorities and the European Commission. We summarize it in this article!
Conference on New Medical Devices Regulations (RMD)
The 6th annual Conference on New Medical Devices Regulations organized by the (EAAR) on the 2nd and 3rd of February 2022 will cover many of the topics of high relevance in the medical devices industry. Want to know more? Visit our page!
New cybersecurity obligations under Radio Equipment Directive (RED)
On October 29, 2021, the European Commission adopted a delegated act to the Radio Equipment Directive aiming at scaling up the cybersecurity of wireless devices and products for the benefit of consumers. Want to know more? Visit our page!