As liquid biopsies, wearables, multi-omics, and AI mature, diagnostics could become the operating system of healthcare: a continuously learning layer that turns everyday data into earlier action.

Manufacturers must cut decision delays, harness AI to unlock messy data, embrace adaptive automation, and empower teams to act as force multipliers. See how these shifts define the path to resilience.

AI is reshaping quality in life sciences, but many teams struggle to balance innovation with audit readiness. Learn how industry leaders are managing risk and building confidence with AI.

The digital revolution that resulted in the Internet of Things (IoT), Internet of Medical Things (IoMT), Software as a Medical Device (SaMD), and connected devices permeating the healthcare ...

Because of their high-speed, repeatability, and long life cycles, INK solenoid valves by the Lee Company are ideal for replacing valves in existing printers, or in new drop-on-demand and dispensing ...

Artificial intelligence (AI) and machine learning (ML) are redefining healthcare, from enabling earlier diagnoses and personalized treatments to streamlining hospital operations and accelerating ...

In 2023, the FDA made the electronic Submission Template And Resource (eSTAR) mandatory for most 510(k) submissions. Although eSTAR is not an AI tool, the move was the first definitive leap toward the ...

Fischer Connectors offers the new Fischer LP360™ connector as the first product of the Fischer Freedom™ Series. This connector facilitates integration, maximizes usability, and optimizes cable ...

Many manufacturing execution system (MES) deployments still operate like it is 2005: a big install, disruptive upgrades, etc. Here's a clearer path forward. International Society for Pharmaceutical ...

AI-assisted symptom recognition and pattern matching leverages machine learning to analyze vast amounts of medical data, including patient histories, clinical notes, and research publications, to ...

The FDA proposed on Feb. 22, 2022, an update to the Quality System Regulation 1 that was released in 1996. The proposal is to reference ISO 13485:2016 Medical devices — Quality management systems — ...

The European Union’s Medical Device Regulation (MDR 2017/745) and In Vitro Diagnostic Regulation (IVDR 2017/746) impose stringent requirements on all economic operators involved in the supply chain of ...