I3CGlobal The core concept of FDA 510k software medical device clearances I3CGLOBAL is a trusted regulatory consulting firm spe ...

Expanding Regional Expertise and Localized Solutions to Meet the Growing Demands of Asia-Pacific Healthcare. The Nelipak ® ...

Expanding Regional Expertise and Localized Solutions to Meet the Growing Demands of Asia-Pacific Healthcare. CRANSTON, RHODE ISLAND US – Media OutReach Newswire – 7 April 2025 – Nelipak® Corporation ( ...

As the Idaho Legislature ended the 2025 legislative session on Friday, lawmakers quickly passed a reworked version of a ...

Judge Sean D. Jordan of the U.S. District Court for the Eastern District of Texas issued an opinion and judgment in ...

As Wilson Sonsini previously reported,1 the U.S. Food and Drug Administration (FDA) had been preparing the industry to comply with the 2024 LDT ...

Jabil experts who worked on the Qfinity reusable autoinjector offer sustainable design advice for high-volume drug delivery ...

For over four decades, the medical device industry has wrestled with fragmented data exchange and proprietary integrations.

After a finding by state authorities that a series of failures and neglect led to the untimely death of a patient in the Kaweah Health Medical Center emergency department, the family of the dead man ...

Given the calls for change, criticism, and ongoing consultations, this article sets out the current status of developments ...

The document addresses facility design, transport vehicle considerations, and personnel considerations for the entire process ...

Lobby groups like AdvaMed and the American Hospital Association have so far failed to get medical devices and critical ...