In the EU, the AI Act has been approved, carrying significant implications for medical device, technology, and pharmaceutical firms. In the US, ...

The Centers for Medicare and Medicaid Services ("CMS") published a final notice outlining the processes and procedures for the Transitional ...

Pakistan Pharmacists Association (PMA) has urged to take immediate action against the illegal import, unlicensed ...

Global logistics expansion and alternative solutions help medical OEMs maintain momentum. ROMEOVILLE, ILLINOIS / ACCESS Newswire / January 30, 2025 / Formerra, a leader in performance materials ...

AI in drug development is a vague term that might mean many things, and today, Owkin is announcing it has enrolled the first patient in a phase 1 study of OKN4395, its “AI-optimized” candidate for ...

Clinical data management companies play a crucial role in the healthcare sector by ensuring the accurate collection, ...

The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with ...

The COVID-19 pandemic forced investigators conducting clinical trials to use decentralized elements, such as telehealth, to ...

The US Food and Drug Administration has released draft guidance on protocol deviations, but experts say it could go further.

Proposed regulations may require employers to invest additional resources to safeguard group health plan participants’ ...

Siemens’ Closed Loop Quality and Compliance for Medical Devices solution facilitates uninterrupted traceability of the compliance approach, ensuring preparedness for recalls and comprehensive control ...