Join our latest Webinar about IVDR. Davide Turchi, Manager of the Regulatory Affairs department at Obelis Group, will walk you through all the challenges related to Legacy Requirements!
Join our latest Webinar about IVDR. Davide Turchi, Manager of the Regulatory Affairs department at Obelis Group, will walk you through all the challenges related to Legacy Requirements!
Join our latest Webinar about EUDAMED. Sandra Ferretti, CCO at Obelis Group will walk you through all the challenges related to Actor and Device Registration!
In this webinar, our top experts suggest strategies and best practices.
The Directive 2010/63/EU on the protection of animals used for scientific purposes aims to replace, reduce, and refine the use of animals used for scientific purposes
The elimination of barriers and the introduction of free movement of goods, services, and people across the Member States have granted a more dynamic business environment. To learn about the consequences of these new changes visit our page!
In this webinar, we will go through the requirements to comply with the European Cosmetics…
Find out more information on the new EU requirements on labels for cosmetics with a special focus on environmental aspects
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
In this webinar we will provide you with an overview about the definition of product information file and also the elements that must include