Learn more about the objectives and main amendments of new EU Waste if Electric & Electronic Equipments regulation 2012/19/EU.
Learn more about the objectives and main amendments of new EU Waste if Electric & Electronic Equipments regulation 2012/19/EU.
Develop a roadmap towards obtaining a CE mark and compliance program for your PPE with Obelis' European Authorized Representative services.
EU vote confirms cranberry products are not medical devices. This is the first borderline product ruling adopted based on MDD 13(1)(d).
New EU Commission Directive 2017/898 is set to enforce higher restrictions on Bisphenol A (BPA) in toys in the interest of consumer safety in Europe.
Understanding the process for products that have been found to be non-compliant with EU Cosmetics Regulation 1223/2009 and the consequences of non-compliance
The Rapid Alert System (RAPEX) is an EU-wide vigilance platform for general products. Learn more about what it is and what it does with Obelis.
The European Court of Justice, by request of Germany's Federal Supreme Court, will clarify the liability of notified bodies in relation to medical devices.
The New Approach Directives are a series of legislative requirements that ensure product safety within the EU market across a range of products and devices.
Representatives from Obelis' European Responsible Person Center and EU regulatory team will be attending Cosmoprof Asia from November 12-14, 2014.
EC publishes revised Blue Guide on implementation of product rules to reflect modernization and harmonization of legislative framework for product marketing.