The regulatory frameworks in the life sciences and healthcare sector keep evolving rapidly and dynamically. Several important legislative reforms ...

MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...

For those with Class IIa or above AI-related devices, compliance with the EU’s AI Act is likely to be akin to the EU MDR.

Arterex, a global medical device design, development and contract manufacturing company, has acquired Phoenix S.r.l., a ...

Top Western and Middle East diplomats and ministers met to discuss sanctions relief for Syria after al-Assad’s removal.

On January 21, 2025, the Council of the EU adopted the European Health Data Space Regulation (the “EHDS Regulation”). The EHDS Regulation aims at making cross-border exchange and access to EU health ...

Pharma: Launch of Shortages Monitoring Platform, several Changes re Clinical Trial Management in EU Countries; Devices: Resolution on the need ...

Cybersecurity has become a leading priority for manufacturers of embedded systems and IoT devices. The rapid proliferation of ...

Arterex said the deal expands its capabilities in medical device development, finished device assembly and packaging to ...

In his March 2023 budget, the then UK Chancellor, Jeremy Hunt, accordingly announced that from 2024 the Medicines and ...

The millions of people residing in urban, semi-urban, rural, and remote areas, the lack of adequate healthcare infrastructure ...

The FDA is particularly concerned that supply chain issues are having an adverse impact on neonatal and paediatric patients.