Lab Compliance

Creating Validation Documentation for BIOVIA Applications

5 December, 2017

Computer systems have produced significant changes to business processes in every industry […]

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What the New FDA Guidance on Electronic Records and Signatures Means for Clinical Trials

28 September, 2017

The digital age is upon us. The FDA has acknowledged the increasing […]

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What the FDA’s Quality Metrics Reporting Program Means for Your Lab

1 August, 2017

Quality metrics are utilized throughout the pharmaceutical industry to assure product quality […]

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Academic Institutions and Regulatory Compliance in the Labs: Why it Matters

27 February, 2017

Partnering and the Challenge of Research Compliance Major research institutions and academic […]

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A Selection of Current Customers