60%Less testing timeCase Study · Medical Device
A clinical-stage biotechnology company replaced manual, paper-based processes with a validated Microsoft Dynamics 365 ERP system and automated validation, delivered on time and within budget.

Paper-based processes, a mandatory ERP validation, and a need for 21 CFR Part 11 compliance before the company reached commercial stage.
CloudMaster 365™ for Microsoft Dynamics 365, ValidationPro℠ services, and the ValidationMaster® platform.
The ERP system went live on time and within budget, with a 60% reduction in test preparation.
At the clinical stage of drug development, every minute counts. This life sciences company selected Microsoft Dynamics 365 for Finance and Operations (D365) as its Enterprise Resource Planning (ERP) system, and the nature of its business made ERP system validation mandatory.
Company executives wanted the foundation for automation in place early, so automated processes would be ready when the company was fully commercial with products on the market. They also needed to achieve 21 CFR Part 11 compliance. While a system integrator implemented D365, the company chose OnShore Technology Group to provide independent validation and verification (IV&V) services and deliver a turnkey validated ERP system within budget.
OnShore Technology Group delivered a three-part solution while the system integrator implemented the ERP system:
The team also helped develop Standard Operating Procedures for ERP system and validation process governance, which are now fully automated.
The client established the automation that sets the foundation for future validation success and has re-engaged OnShore Technology Group to help keep the system in a validated state.
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