Will your products be compliant with the European Union (EU) Medical Device Regulation (MDR) when it takes full effect on May 26, 2020? Since the intr...
Europe Bans Halogenated Flame Retardants in Plastic Enclosures & Monitors
On October 1, 2019, the European Union (EU) adopted Regulation (EU) 2019/2021, a package of ecodesign requirements for electronic displays. The regula...
Ask the Experts: December 6 Edition
Our regulatory subject matter experts are always helping a range of stakeholders solve compelling regulatory challenges associated with supply chain d...
The Scope of the EU Medical Device Regulation
The European Union (EU) Medical Device Regulation (MDR) is due to take full effect in May 2020, and its new scope includes a large number of products ...
Understanding Section 10.4.1 of the EU MDR
After a three-year transition period, the European Union (EU) Medical Device Regulation (MDR) 2017/745 is set to take full effect on May 26, 2020, rep...
Assent Enhances Global Presence With Offices in Europe & Asia
Today, Assent announced its expansion into the European Union (EU) and Asia, with new office locations in Amsterdam, Netherlands, and Penang, Malaysia...
European Commission Announces New Consultations on Proposed RoHS Directive Exemptions
The European Commission (EC) has launched four public consultations on proposed exemptions to the Restriction of Hazardous Substances (RoHS) Directive...
What Changes Are Coming to EU ErP Directive in 2016?
The European Union (EU) is currently discussing possible changes to its Energy-related Products Directive (2009/125/EC). In the EU, Directives provide...