Data Integrity

Data Integrity

Regulatory agencies expect all areas of GxP, including clinical trials, QC labs, and the manufacturing process to be in a “state of control” and this control includes how data is recorded. The FDA requires companies to validate any application that’s part of the overall quality system. As the US FDA has stated: “data integrity is an important component of industry’s responsibility to ensure the safety, efficacy, and quality of drugs, and of FDA’s ability to protect the public health.” UL’s Data Integrity program, which includes eLearning courses from industry-leading subject matter experts, as well as hands-on consulting activiites, enables companies to build awareness to the entire GxP audience, including QA, QC Lab and IT professionals.

Courses in this Program