Webinars and events Archives

Webinar – Adverse event reporting for cosmetics in the US market: addressing serious incidents and reporting to the FDA

Book your spot for our new live webinar about adverse event reporting for cosmetics in the US market, on September 19th

Webinar: new USA Cosmetics Regulation Act (MoCRA): How to safely pass the deadline!

Discover the NEW USA Cosmetics Regulation Act (MoCRA) and ensure a seamless transition with our upcoming live webinar!

Webinar: (New)MDR Legacy extension: EU, UK and CH

Register to our new webinar to learn about the MDR Legacy extension in EU, UK and CH. Register now!

Webinar: Steps to enter the Australian market for Medical Devices

Manufacturers! Interested in the European Commission proposal for legacy devices? Our consultant will be offering an interpretation of the European Commission proposal for legacy devices regarding the following date: March 20, 2023

Obelis Group to support small medical device companies in Luxemburg’s Fit 4 Innovation Programme as Regulatory Consultant

We are thrilled to announce that Obelis Group has been chosen as one of the regulatory consultants for the Luxemburgish Ministry of Economy’s Fit 4 Innovation

Seminar: Placing Medical Devices and In-Vitro Diagnostic Devices on the Union Market (EU) – News and Challenges

Medical Device and In-vitro Diagnostic Industry Discussion: Key Takeaways on IVDR and MDR Implementation Challenges

Obelis partner regulatory training: takeaways from Chemron FDA Korea

An interview with Sarah You about her experience in following one of our expert’s professional trainings on EU Regulations and the insights she gained from it.