Quality Management Systems (QMS) are integral for medical device manufacturers as they ensure adherence to regulations and help in producing top-quality products. Utilizing the right QMS software ...

medical devices often don't have built-in tools for software upgrades when a security patch becomes available. Healthcare CIOs face challenges in capturing a comprehensive inventory of medical and ...

On 11 December 2024, the MHRA published a revised roadmap for the long-awaited reforms to the UK Medical Device Regulations 2002 (MDR Roadmap).

Venudhar Rao Hajari has built a successful career in the areas of Medical Device Development Quality Assurance, Software ...

These include deficiencies in Software Bill of Materials (SBOMs ... beyond regulatory compliance—they’re reframing the medical device industry’s approach to cybersecurity.

The Ministry of Food and Drug Safety approved the software medical device for depression probability assessment (product name ...