Contract manufacturers have special expertise in the characterization and validation of biopharmaceutical manufacturing processes. Process development is a key factor in the development and ...

Critical process parameters (CPPs) and their associated process controls are crucial to drug development and process validation and to the evaluation of every manufacturing unit operation. The ...

In this GEN webinar, our expert speaker, Matt Taylor, discusses how pre-packed chromatography columns can provide reliable small-scale models of the downstream mAb purification process.

MOUNTAIN VIEW, Calif., April 21, 2021-- Synopsys, Inc. (Nasdaq: SNPS) today introduced at SNUG ® World international user conference, PrimeLib ™, a high-performance, comprehensive characterization and ...

Expertise in CMC (chemistry, manufacturing, and control) ensures the appropriate manufacture of a pharmaceutical or biologic by coordinating material characterization, formulation development, and ...

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 ...

In today’s highly regulated environment for drug development and manufacturing, new challenges have emerged from internal pressures to reduce costs by eliminating waste in the development process, ...

Variation modeling has evolved over the past several years from a single derating factor that represents on-chip variation (OCV), to Liberty Variation Format (LVF), today’s leading standard format ...