LIMERICK, Ireland, Oct. 31, 2024 (GLOBE NEWSWIRE) -- kneat.com, inc. (TSX: KSI) (OTC: KSIOF), a leader in digitizing and automating validation and quality processes, is pleased to announce that a ...
ProMed, a leading contract manufacturer specializing in medical-grade silicone and plastic components, provides comprehensive support for medical device, pharmaceutical, and combination drug-device ...
Using a combination of plasma and urine biomarkers along with serum PSA in predicting prostate cancer and screening for high-risk cancer. This is an ASCO Meeting Abstract from the 2014 ASCO Annual ...
FDA’s 21 CFR Part 820 — Quality System Regulation (QSR) has not been updated since it was first released in 1996 . . . until now. Are you ready? Part of a panel at the conference discussing the ...
LONDON, October 28, 2025--(BUSINESS WIRE)--European medical device companies are carrying out digital transformations to modernize regulatory operations, strengthen post-market surveillance and ...
Figure 1. Preclinical testing and clinical testing must be part of this generic product development cycle (click to enlarge). Contract research organizations (CROs) used to be considered premarket- or ...
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