Autonomous and automated systems are increasingly being used across domains. Yet, the distrust in their reliability is growing due to lack of transparency, which will reduce acceptance and slow down ...

This article is a condensed version of an article that appeared in the November/December 2022 issue of Chip Scale Review. Adapted with permission. Read the original ...

Dublin, Feb. 27, 2025 (GLOBE NEWSWIRE) -- The "3hr Virtual Seminar - Validation, Verification and Transfer of Analytical Methods - Implementing Guidelines from FDA/EMA, USP and ICH" training has been ...

Inadequate process validation is one of the most common issues leading to warnings from the US Food and Drug Administration (FDA). It may also be the most difficult to address, according to Max ...

Maintaining a healthy quality system and complying with the Food and Drug Administration’s expectations has never been more important for manufacturers making medical devices bound for the US market.

In his 1996 review of analytical method validation, author Mark Green notes, “Doing a thorough method validation can be tedious, but the consequences of not doing it right are wasted time, money, and ...

All methods of analysis must be validated, and peer reviewed prior to being issued. Each EPA office is responsible for ensuring minimum method validation and peer review criteria have been achieved.

As semiconductor devices continue to advance, the demand for reliable, high-performance test sockets has never been greater. Yet, traditional socket design validation methods—such as per-pin ...