Obelis Chief Compliance Officer, Mrs. Sandra Ferretti, participated in the official inauguration of CURAM – Center for Research in Medical Devices, which took place on Monday, the 26th of September 2016 in Galway, Ireland. The event, co-organised by Dr James J. Browne, the President of NUI Galway and Professor Abhay Pandit, the director of CURAM, brought together world-class academic, medical devices industry and clinical partners.
Obelis officially launched a new scientific department. It aims to aid manufacturers and help spread awareness around obligatory compliance issues.
EU publishes new harmonized standards for Radio and Telecommunication Terminal Equipment in Europe. Talk to Obelis to find out how they may affect your product.
Obelis launches new registration and EAR service for non-EU manufacturers seeking to introduce medical and in-vitro diagnostic devices on the Croatian market.
What is the compliance path for EMC & LVD products when trying to bring a wide range of products to the European market? Read on the compliance process here
From April 2016, low voltage directive 2006/95/EC will be repealed by the new 2014/35/EU LVD.
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.
More info on required criteria for awarding the Ecolabel to rinse-off cosmetic products within the EU-a voluntary label promoting environmental excellence.
EU introduces new radio and telecommunications directive 2014/53/EU to replace current legislation. The directive will enter into force in June 2016.
Newly adopted EC regulation EU 207/2012 will introduce a new electronic labeling requirement for medical devices on the European market.