Two-day seminar delivered by top industry experts! Aimed at providing basic knowledge and concepts to those who are interested in the role of Person Responsible for Regulatory Compliance (PRRC).
Two-day seminar delivered by top industry experts! Aimed at providing basic knowledge and concepts to those who are interested in the role of Person Responsible for Regulatory Compliance (PRRC).
Medical device trade is affected by MDR and lack of MRA update. Find out all the details!
Obelis group, in collaboration with Beauty Independent, produced a roundtable on the cosmetics compliance requirements to access the EU & the UK markets.
Find out more information on the new requirements by MDR and BREXIT
The upcoming IVDR regulation will be fully applicable as of May 26, 2022. There will be changes in the IVDR landscape, and manufacturers must make sure to be compliant on time, in order to keep selling their devices on the European market.
The new medical Device Regulation is fully applicable as of May 26, 2021, therefore you need to know how to manage your Legacy Devices Compliance in the EU.
The cosmetic industry has experienced a significant rise in the presence of cannabis-based ingredients. Find out more about restrictions and use.
Discover the new methods of evaluation through CORE-MD project on high-risk medical devices in Europe.
In the webinar we provide an overview of MDR review process for Software, MDR Class I software, MDD Class I Software with class upgrade under MDR and more
European Commission’s European Green Deal aims at transforming production and consumption of products on the EU market, in order for them to become more durable, resilient and eco-friendly.