ACM Global Central Lab Platform Now CDISC Compliant
Rochester, NY, Jan. 28, 2010 –
The Web-based platform is available on a global basis. Access is fully secure and compliant with FDA regulations, requiring proper login information for authorized individuals. Users can schedule automatic reports and receive alerts in their email when the reports are accessible. Per-subject reports are available for trial investigators and per-study reports offer sponsor analysis on enrollment status, test result trending and summary data, among many other variables. Furthermore, LabStar’s robust ad hoc reporting enables users to analyze data by any result, demographic or therapeutic detail.
“Serving our customers and providing state of the art solutions is always ACM’s priority; so much so that we formed a customer advisory committee. We value their input and strive to provide optimal solutions,” said Elena Logan, VP of Clinical Trials, ACM Global Central Lab. “We are excited to offer our clients a much more flexible, highly intuitive solution that allows them access to their lab data.”
LabStar is a value-added service that empowers users to achieve optimum protocol efficiency. Closing managing and monitoring a protocol can save time and money by making decisions with real-time results. LabStar data is in strict accordance with GCP and HIPPA regulations and now enables convenient feedback to ACM for training requests, technical issues or suggestions for continual improvement.
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