Friday, March 24, 2017
 

Life Sciences

Clinical Research
 

Good laboratory practice (GLP) requires quality guidelines that ensure the safety and efficiency of the facility's research. Reliable equipment must be routinely audited and temperature data logged and archived to meet stringent AAALAC standards.

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Pharma/Biotech
 

Maintaining specific environmental conditions is crucial for the safety and purity of pharmaceutical and biotech products. Manual medical monitoring and recording is time-consuming and a poor use of highly qualified resources.

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Fertility
 

Assisted reproductice technology clinics deal with very personal and delicate issues that demand accurate and reliable equipment to assist in managing and adhering to CLIA standards. It's required that all ART practices participate in the CDC registry data collection and must document and archive temperature data.

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