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June 15, 2015
A new GMP facility in Massachusetts will produce enzymes and other reagents for in-vitro diagnostics.
June 09, 2015
Lyophilization Services of New England announces inspection approvals that will allow its Bedford, NH facility to begin manufacturing commercial drugs for US distribution.
June 08, 2015
Designed with safety standards in mind, flowtherm Ex incorporates a number of connectable sensors, such as vane wheel, vortex, thermal, Pt100, and other physical sensor with analog output, thereby allowing a range of applications.
June 02, 2015
Clearly defined zones of cleanliness must be designed and maintained to prevent product contamination.
Careful choice of wash-water parameters and attention to water quality and basket loading are important for optimal cleaning.
May 27, 2015
This new pharmaceutical stability storage facility will enable the company to expand its analytical and formulation offerings to the pharmaceutical and biotech industries.
May 20, 2015
The Denmark facility will incorporate CMC’s Bioreactor 6Pack configuration in one manufacturing line.
May 15, 2015
Traditional sterility testing methods can take 14 days or longer to complete, so a growing number of pharmaceutical manufacturers and quality control
Total cost of ownership, including operating costs, must be considered when deciding between flexible and traditional cleanroom systems.
Aging facilities and inadequate quality systems create drug shortages. Preventing them will require harmonized regulations, and management support for continuous improvement and innovation.