Find out more information on the European Directive increasing the safety requirements for cosmetic products.
Pressure equipment
The impact of the new MDR and IVDR Regulations on Notified Bodies
The new MDR (2017/745) and IVDR (2017/746) will replace the EU’s current Medical Device Directive (MDD) (93/42/EEC) and In Vitro Diagnostics Directive (IVDD) (98/79/EC) to establish a more robust EU legislative framework and ensure better protection of public health and patient safety.
The PPE Regulation countdown is about to start
Learn all you need to know about EU PPE Regulation 2016/425 before it enters full effect on April 21st 2018. Talk to Obelis' experts about your compliance.
What is CE Marking?
A definitive guide to CE marking in Europe. Discover what a CE marking is, what products require a CE mark, and why a CE mark is required on the EU market.
New Pressure Equipment Directive
The new EU Pressure Equipment Directive (2014/68/EU) will come into effect from July 2016. Talk to Obelis about what implications it may have for your product.
Exporting to Europe – “Selling” is not Complying
In many cases it is possible for some products to have found their way onto the European Market without having undergone the proper Compliance screening processes or having been awarded an official CE Marking. In these types of cases, manufacturers may well feel that there is no real pull factor to encourage them to seek CE certification and that the onus to request information on such issues falls outside the realm of their responsibility.