Italy enacts decree requiring in-vitro diagnostics device manufacturers with devices on the Italian market to register products with health ministry database.

Italy enacts decree requiring in-vitro diagnostics device manufacturers with devices on the Italian market to register products with health ministry database.
EC publishes revised Blue Guide on implementation of product rules to reflect modernization and harmonization of legislative framework for product marketing.
EU introduces new radio and telecommunications directive 2014/53/EU to replace current legislation. The directive will enter into force in June 2016.
The EC proposed new personal protective equipment (PPE) regulation to replace current EU legislature and harmonize Europe-wide standards and requirements.
New EU implementing regulation 920/2013 to set more stringent requirements for the designation and supervision of Notified Bodies within Europe.
Learn more from the experts at Obelis on how to write successful cosmetic claims for products on the EU market under regulation 655/2013.
More information on cosmetics notification and compliance issues in the transition period from Cosmetics Direction 76/768 to EU Regulation 1223/2009.
The EU Commission has published a new legislative framework package for the marketing and advertising of CE marked products on the European market.
Obelis and Israeli Chamber of Commerce organise EUCORE event for cosmetics manufacturers looking to introduce products to the EU market.
EU Commission revises 700 Old Approach directives and 27 New approach Directives. Read about these topics here.