The Nigerian Midstream and Downstream Petroleum Regulatory Authority (NMDPRA) has recommended stricter measures for fuel ...

The newly signed India-UK trade agreement introduces a mutual recognition framework facilitating seamless entry of Indian ...

Hohenstein Medical said the Good Laboratory Practice certification expands its ability to support regulatory needs of device manufacturers.

India-UK trade deal eases market access for Indian medical devices in the UK. Zero tariffs and mutual recognition agreements ...

NATHEALTH highlights the need for regulatory reforms in India's healthcare sector, pointing out compliance bottlenecks and ...

Products certified by CDSCO and ICMED will now face fewer regulatory barriers, boosting Indian competitiveness in the British ...

A clear intellectual property and product risk evaluation strategy helps device companies with investments and M&A.

Artificial intelligence (AI) in health care is rapidly advancing beyond traditional applications. Autonomous AI agents are ...

Designing medical devices for such varied use cases requires more than just technical proficiency. It calls for strategic ...

ClariMed, Inc., a global leader in human-centered medical device development and regulatory services, today announced it has achieved ISO 13485:2016 ...

There’s no questioning that AI should have governance and guardrails. As much good as it can bring, it also heightens risk.