(“Glucotrack” or the “Company”), a medical device company focused on the design, development, and commercialization of novel technologies for people with diabetes, today announced that it ...

This certification demonstrates Signifier’s commitment to meeting the highest standards of safety, performance, and efficacy required by the European Union for medical devices. The EU MDR ...

CMOs can solve challenges with state-of-the-art equipment and expertise, explains Henri Asselin at Beacon MedTech Solutions.

One area that medical device manufacturers often overlook in post-market surveillance (PMS) planning for EU MDR and EU IVDR ...

China has issued a guideline on comprehensively deepening the reform of regulation of drugs and medical devices to promote the high-quality development of the pharmaceutical industry, the National ...

On 21 st January 2025, the EU Council approved the EU Health Data Space Regulation (the " EHDSR "). This will come into force ...

The University Grants Commission (UGC) has released a list of medical colleges that have been issued show cause notice for not complying to Anti Ragging Regulations 2009 for preventing ragging at ...

MLMD are subject to the act and associated Medical Devices Regulations (regulations). In this guidance, "transparency" describes the degree to which appropriate and clear information about a device ...