The regulations for establishing, implementing, and maintaining GCP compliance can be overwhelming. Companies face many challenges in controlling required documentation and managing processes during clinical studies. With MasterControl, the processes involved in satisfying GCP compliance requirements can be simplified and streamlined.
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For more than a decade, MasterControl has provided configurable, easy-to-use quality management software solutions that keep companies’ clinical quality processes connected and properly aligned with the most current GCP compliance requirements, such as the ICH GCP E6 R2 Addendum, which encourages implementation of improved and more efficient approaches to clinical trial design, conduct, oversight, recording and reporting while continuing to ensure human subject protection and reliability of trial results.
GCP compliance requires companies to be compliant, connected, and complete.