See How Pharmas and Drug MFGS Use Trievr for the New FDA Quality Metrics Program

Here’s How it Works:

Using TRIEVR’s QM data collection forms and data request management features, you first identify your MFG teams, establish your request schedule from daily to quarterly time periods, set a due date and release.
TRIEVR will alert the MFG teams and provide them with an on-line form to enter the QM data.

If your MFG teams make hundreds or even thousands of lots in the time-period, no problem, TRIEVR provides an upload process that allows large volume MFGs to efficiently provide the data back to you. The data is immediately posted to the secure and encrypted central database. Your QM data is available in real time to export, review and report.

Why major pharmas use Trievr to simplify their work and meet the FDA Quality Metrics requirements.

If you are a pharmaceutical company or drug manufacturer, you’ve probably heard of the quality metrics program being developed. This program began in 2013 to help pharmas and their manufacturers CREATE A STANDARDIZED QUALITY METRICS SYSTEM so that the FDA could collect quality data in lieu of or in advance of inspection.

These quality metrics include number of lot release tests, out-of-specification results, and lots attempted, rejected, reworked, and reprocessed.

While the FDA QM Program is NOT projected to be released UNTIL early 2018, MANY TOP PHARMACEUTICAL COMPANIES have already BEGUN ROLLING OUT THE QM PROGRAM USING TRIEVR’s Request management cloud platform with quality metrics forms already built in.

Pharmas use TRIEVR so they can work with 3rd party and internal departments to help send out, remind, and manage the QM data collection. They can then analyze ALL – in REAL TIME – with Trievr’s DASHBOARD & REPORTING TOOL.

All of this is easy and efficient.

For more information and to schedule a demo,  contact us today!

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