Find out more information on the new EU requirements on labels for cosmetics with a special focus on environmental aspects

Find out more information on the new EU requirements on labels for cosmetics with a special focus on environmental aspects
In this webinar, we will be providing you with information about the UK MHRA Medical Devices & IVDs registration process registration
We met with over 400 manufacturers from more than 50 countries in MEDICA’s halls. Here are the latest news and insights we got from medical manufacturers.
In this webinar, we will provide an overview of the role of the Responsible Person in UK and the notification process
This webinar walks you through key milestones as your company prepares for the IVDR date of application in May 2022!
In this webinar we will provide you with an overview about the definition of product information file and also the elements that must include
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