Did You Know...

That a streamlined IT system could increase end-to-end trial visibility and accelerate clinical trials by 10 percent or more?


According to a recent article in The McKinsey Quarterly entitled “Using IT to Speed Up Clinical Trials,” pharmaceutical companies spend hundreds of millions of dollars on clinical trials that may take up to seven years to complete. When pharmaceutical companies manage regulatory processes with the latest organizational technology, they are able to connect people with the documents and information they need when they need it. True end-to-end solutions for collecting, organizing, and reviewing all the documents required to meet industry GCP standards are found by connecting operations and technology in a visible format that management can easily utilize. Streamlining approval cycles with an automated system can help companies find, collaborate, and approve work instructions, SOPs and other controlled documentation.

Read more about the benefits of streamlining and automating process and content management operations:

White Paper:
SOP Management as a Compliance Tool in FDA and ISO Environments

Product Data Sheet:
MasterControl GCPDocs Spark?



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