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How CLSI standards help international manufacturers navigate FDA regulatory approval with confidence
In this guest editorial from the Clinical and Laboratory Standards Institute (CLSI), explore FDA clearance pathways and how CLSI standards can help expedite regulatory approval
The SIFT-MS mobile laboratory: Pollution source identification
Lonza to expand bioscience testing offering with the acquisition of Redberry
Acquisition to include Red One™ solid-phase cytometry platform for rapid sterility and bioburden testing, which expands Lonza’s portfolio of automated, scalable solutions for pharmaceutical quality control
Transforming workflow efficiency through affordable robotic automation
BUCHI introduces a new freeze-drying system developed for R&D environments
The timesaving Lyovapor™ L-210 sets new efficiency standards while maintaining reliable and stable cooling performance
Teva and Prestige Biopharma enter license agreement for Tuznue commercialization in Europe
Tuznue is a biosimilar of Herceptin (trastuzumab), developed to offer a more cost-effective therapeutic alternative for patients
Biomarker discovery service
How FcRn mouse models from JAX reveal antibody half-life and stability
Advancing clinical pharmacokinetic prediction beyond non-human primate models
Key highlights at ELRIG Drug Discovery 2025
Guide to Good Pipetting
Automated cell counting drives development of novel therapeutics
Discover how researchers are using the LUNA-FX7™ automated cell counter to deliver precision and compliance in modern biopharma workflows
























