Clinical Regulatory Quality and Document Management Platform for the Life Sciences Industry

This client is a compliance management software company based in Europe that specializes in developing cloud-based enterprise software for the life sciences industry, medicines agencies, and national competent authorities. The company had an existing SharePoint application that was used for drug quality assurance, but it was not scalable and had several other limitations including licensing issues, costly maintenance, and so on. The client’s goal was to replace their existing application with a dynamic and customizable platform.

The e-Zest team leveraged their expertise in Angular and .net to develop a web-based, dynamic platform that could be customized as per Excel configurations. With this platform, the client could configure multiple applications under one application (QMS, DMS, eTMF) and scale it as and when required. It also helped the client to achieve substantial cost savings by eliminating the necessity to renew licenses and allowed them to build their own IP using our framework.

Some of the major business outcomes of the project include:

  • Reusable component creation
  • 95% automated features for testing
  • Excel/XML based configuration import engine
  • Excel/XML based configuration workflows for platform
  • WOPI/O365 Implementation
  • End-to-end configurable application for QMS, DMS, and eTMF

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e-Zest is a leading digital innovation partner for enterprises and technology companies that utilizes emerging technologies for creating engaging customers experiences. Being a customer-focused and technology-driven company, it always helps clients in crafting holistic business value for their software development efforts. It offers software development and consulting services for cloud computing, enterprise mobility, big data and analytics, user experience and digital commerce.