eu mdr
Archetype appointed to secure EU Market approval for LumipenPro
Medical illumination device targets EU aesthetics market.
More in eu mdr
Disruptive technologies taking the medical device industry by storm
The medical device industry is poised to benefit from greater agility and long-term efficiency savings.
EU IVDR clinical evidence requirements
New RQM+ paper highlights overlap in EU and US requirements to support efficient compliance.
3 steps to more connected clinical trials
New strategies are enabling better collaboration with sites, improving the patient experience, ensuring data quality, and driving greater inspection readiness.
RQM+ brings IVDR thematic search tool free to market
To help increase compliance efficiency, a new, freely available IVDR filtering tool is being offered to the market by RQM+.
Helping medical device manufactures navigate the new EU MDR
Trelleborg and other industry experts explain the material-related requirements of the MDR and how to achieve them.
EU MDR mandates require more than ad-hoc manual processes
How medical device manufacturers can make labeling operations compliant for European markets.
