As the saying goes, if it looks too good to be true, it probably is.
This online series of workshops will arm you with the information you need to overcome challenges and achieve compliance with EU MDR.
Label and packaging artwork processes play an important role in meeting compliance for EU MDR.
By simplifying labeling compliance, companies can focus on better serving current and new markets.
Upgrading your enterprise labeling system could play a key role in ensuring compliance.
U.S. medtech manufacturers must also prepare for the UDI requirements under EU MDR.
Using automated technologies can help medtech manufacturers de-risk their supply chain, increase productivity and save costs.
Reduce risk and control your label, its design, and the data.
How simple labeling changes can drive big results for medical device manufacturers.
The agency wants to make sure that all patients receive information about the risks of the female contraception device prior to implantation.