Non-Viable Particle Testing

Articles & Whitepapers

USP 797 Environmental Monitoring 101 - HVAC Requirements

USP 797 is a standard for sterility that pharmaceutical compounding and preparation facilities must demonstrate. USP 797 is set by the United States Pharmacopeia and National Formulary (USP-NF) and ensures patient safety by protecting pharmaceuticals from contamination during preparation. Following USP 797 reduces infection, contamination, and improper dosage to maintain superior quality products ...

5 Key Principles of Cleanroom Particle Counting

Cleanroom particle counting is essential for accurate functioning and meeting certification criteria in controlled environments. In this blog post, we take a look at five key principles of cleanroom ...

CD Formulation Enlarges Particulate Matter Testing Capability for Drug Formulation

The safety of a medicine is of vital importance to the safety of patients. Many factors may affect drug safety during pharmaceutical manufacturing. As a New York-based CRO company, CD Formulation always gives high priority to drug safety issues and ...

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Compressed Gas Kit for Viable Particulate Monitoring

Compressed gases are viewed as critical utilities in many industries when in direct product contact or in the clean room environment. Control of the environment where Pharmaceutical and Cosmetic products are manufactured is a key element of ISO and GMP Standards worldwide. The absence of viable contamination is considered a critical quality attribute due to its potential to dramatically impact ...