Integrated PrimeSim simulation technology, PrimeTime signoff STA validation and SmartScaling for multi-PVT yields high-quality libraries for faster design convergence PrimeLib ML and advanced ...
Mutual Customers Gain Up to 5x Reduced Turnaround Time and Golden Signoff-Quality Libraries for Automotive, AI Chipset, Aerospace and Defense, HPC and 5G Markets MOUNTAIN VIEW, Calif., Sept. 22, 2021 ...
Matt Taylor is a senior process development associate at KBI Biopharma, where he focuses on the design, optimization, and scale-up of purification processes for biopharmaceutical manufacturing. Matt ...
Efficient and accurate library characterization is a critical step in full-chip or block-level design flows because it ensures that all library elements perform to specification under all intended ...
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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 ...
Process characterization and viral clearance validation are pivotal studies in biopharmaceutical manufacturing, particularly for monoclonal antibodies (mAbs) produced in mammalian systems, which carry ...
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