Regulated industry insights
Blog A Guide to the New Drug Application Process Since 1938, every new drug of a pharmaceutical company has been the subject of an approved
Blog The Connection Between Using a Document Management System and FDA Compliance Labs that receive FDA warning letters must waste valuable resources to become compliant
Blog In the US alone, organizations are subject to hundreds of regulations from the government and other regulatory bodies. Managing these regulations and staying compliant
Blog Expansion of FDA Data Standardization Rules with FDAs DART Fit For Use Pilot In drug development, the Food and Drug Administration (FDA) issued final
Blog SENDIG v3.1.1 and the FDA Approval Process The cost of developing a new drug can be as high as $2.9 billion. Even after such
Blog The Right LIMS Solution for Your Lab The global market for LIMS software is expected to expand by a massive 7% by 2030 because
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