UK regulatory approval follows FemaSeed, FemVue and FemCerv clearance/ approvals in the U.S., Europe, Canada and ...

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

Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...

DUBLIN--(BUSINESS WIRE)--The "Pharmaceutical Regulatory Affairs Market Size, Share & Trends Analysis Report By Service Provider, By Service, By Category, By Indication, By Development Stage ...

MHRA has published guidance to medical device manufacturers on upcoming requirements around post-market surveillance New regulations come into force on 16 June that mandate more stringent data ...

In the recent draft "Teachers Eligibility Qualifications (TEQ) in Medical Institutions Regulations", the National Medical Commission (NMC) has relaxed some of the norms of teachers' eligibility ...

The draft regulation by the University Grants Commission (UGC) on the selection and appointment of vice chancellors of universities has evoked protests by non-Bharatiya Janata Party-headed State ...

The FDA’s Center for Devices and Radiological Health issued a statement on medical device supply chain vulnerabilities, the public health impact they have on patient care, the FDA’s actions to prevent ...

After a recent Windows update, some users have reported the computer or other devices fail to appear in the network list. Because of that, they are unable to share files and printers between ...

Task force aims to create clear crypto regulatory framework Trump administration seeks to reverse previous SEC crypto crackdown Industry leaders welcome move towards regulatory clarity Jan 21 ...

Big AI companies like Google, Meta, OpenAI and Amazon, have come out hard against comprehensive regulatory efforts in the West — but are receiving a warm welcome from leaders in many other countries.