From July 2014, the national Irish medical and cosmetics regulator, Health Products Regulatory Authority, will become known as the Irish Medicines Board.
Other Industries
Italy Decree on online registration of IVDs!
Italy enacts decree requiring in-vitro diagnostics device manufacturers with devices on the Italian market to register products with health ministry database.
New version of the Blue Guide 2014. What is new?
EC publishes revised Blue Guide on implementation of product rules to reflect modernization and harmonization of legislative framework for product marketing.
New Electromagnetic Compatibility Directive 2014/30/EU
EU to introduce new electromagnetic compatibility directive to regulate compatibility of devices and ensure reduced electrical disturbance and consumer risk.
More Supervision on Notified Bodies by NEW 920/2013 Regulation
New EU implementing regulation 920/2013 to set more stringent requirements for the designation and supervision of Notified Bodies within Europe.
How to write cosmetic claims
Learn more from the experts at Obelis on how to write successful cosmetic claims for products on the EU market under regulation 655/2013.
New Electronic Labeling for Medical Devices
Newly adopted EC regulation EU 207/2012 will introduce a new electronic labeling requirement for medical devices on the European market.
Cosmetic Notification between January 2012 to July 2013
More information on cosmetics notification and compliance issues in the transition period from Cosmetics Direction 76/768 to EU Regulation 1223/2009.
New package of measures for marketing of products
The EU Commission has published a new legislative framework package for the marketing and advertising of CE marked products on the European market.
EROMED Workshop in Sao Paulo a Success!
The two-day EU regulatory workshop included sessions on developments in medical device legislation and manufacturer obligations for the European market.