A global medical technology manufacturer

Upgrading a Fortune 500 med-tech company’s legacy system for FDA’snew regulations

3 ->1

unified platform

100%

regulatory compliance readiness

Faster

workflow automation

A global med-tech manufacturer needed to modernize three outdated legacy systems to meet new regulatory requirements and support long-term operational growth.

Challenge

01

Three outdated .NET 2005 legacy systems could no longer meet new regulatory and labeling requirements.

02

Fragmented architecture slowed development, caused maintenance issues, and created operational inefficiencies.

03

The business faced urgent compliance deadlines and needed a unified, reliable, scalable platform.

Solution

A unified, modern platform to ensure compliance, improve efficiency, and enable future growth.

Tech:

.NET SQL Server

How we worked

01

Consolidated three legacy applications into one modern, web-based platform with updated architecture.

02

Implemented compliant labeling, workflow improvements, reporting, and admin controls.

03

Enhanced performance, unified data, and enabled scalable feature development for future needs.

Result

The legacy systems were successfully unified into a single, modern, regulatory-compliant platform.

The upgraded system met the new regulatory standards (e.g., labeling and compliance requirements) — enabling the client to continue global medical device distribution legally and securely.

Workflow efficiency improved: reporting, approvals and data management became streamlined; manual overhead reduced significantly.

The client gained a maintainable, scalable system foundation — facilitating future development and feature expansion.

Industry

Healthcare, Manufacturing

Services

Custom Development Dedicated Teams

Technologies

.NET SQL Server

Business Impact

PerformanceTime-to-market

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