Want to learn how to SAVE 1000’s of hours communicating your product specs changes to your vast network of manufacturers and suppliers? DO YOU ALSO WANT TO improve your verification of receipt and change implementations – ALL WITHOUT USING DOCUMENTS, SPREADSHEETS OR EMAIL?
SAY HELLO TO TRIEVR
Trievr REMOVES the painstaking manual process of communicating and tracking spec changes to your manufacturers and suppliers. Our FDA GxP compliant SaaS based program serves as the bridge between your specification management system and those who need to be alerted.
Here’s how it works:
Treivr can work with your team to set up secure API connection between trievr and your internal spec system. Trievr will then grab all the new or changed specs, the recipients info, implementation timelines PLUS more and then automatically notify all recipients what actions need to take place. TRIEVR then collects and documents proof of receipt and proof of spec download,making everyone accountable. TRIEVR will automatically remind those who don’t take the necessary actions, until the work is complete. PLUS, YOU CAN MONITOR IN REAL TIME WHERE IT IS IN THE PROCESS THROUGH TRIEVR’S DASHBOARD AND REPORTING TOOL.
With TRIEVR you can go to one place, see the new spec notices, know implementation time lines and direct questions back to the company for clarification.
IF YOU WANT TO IMPROVE COMPLIANCE WHILE ELIMINATING MISSED OR MISMANAGED SPEC REQUESTS, PLUS SAVE 1000’S OF HOURS USING DEDICATED RESOURCES MANUALLY TRACKING SPEC CHANGES WITH LISTS, SPREADSHEETS, EMAIL AND MORE….SIGN UP FOR TRIEVR TODAY.