Trievr to Provide Major Pharmas with Request Management Platform to Meet New FDA Quality Metrics Requirements
SAN ANTONIO, Oct. 16, 2017 /PRNewswire/ -- Trievr, a FDA GxP compliant request management platform, today announced that three of the top 10 major pharmaceutical companies have signed with Trievr to help facilitate and simplify the new FDA Quality Metrics (QM) Requirements. These quality metrics include number of lot release tests, out-of-specification results, lots attempted, rejected, reworked and reprocessed.
Pharmas internal departments use Trievr's QM data collection forms and data request management system to easily work with third parties; such as suppliers and manufacturers, to request, remind and manage the QM data collection. Pharmas can then analyze the data collected in real time with Trievr's reporting tool.
With Trievr, Pharmas can first identify their manufacturing teams, establish a request schedule from daily to even quarterly times periods, set a due date and send out the notifications. Trievr will alert the manufacturing teams and provide them with an on-line form to enter the QM data.
"This is the first platform that is designed to handle 100's to 1000's of lots in the same time period that also allows large volume manufacturers to efficiently provide the data back to the Pharmas," said Greg Brigham, Trievr CEO, "Pharmas, manufacturers and many others use Trievr to help automate requests to retrieve, organize and monitor data requirements that can then be sent to the FDA."
Additional information about Trievr can be found at http://www.trievr.com
About Trievr
Trievr, based in San Antonio, TX, serves organizations seeking a faster and easier solution to manually collect and organize data used for quality metrics, audits, recalls and quality control compliance reports. Founded in 2014, Trievr's FDA GxP compliant SaaS based request management system works outside other systems and serves as a bridge between internal departments and third parties.
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SOURCE Trievr
