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About the Client

The client is one of the world leaders in the development, supply and technical support of formulated film coating systems. With a strong presence in over 26 countries, they excel in modified release technologies and functional excipients for the pharmaceutical industry. They approached Unified Infotech to provide support for all phases of solid oral dose design, development and manufacturing processes.

The Background

Creating new formulations for Pharmaceuticals and Active Pharmaceutical Ingredients is a tedious process that involves keeping track of endless regulatory filings, which is time-consuming and expensive.

To overcome this challenge and help drug manufacturers, the client wanted to build an intelligent, cloud-based application that digitizes the product formulation design, development and approval process. The purpose behind developing this application was to ensure a faster time to market and cost-efficiency.


  • Consulting & Planning
  • Information Architecture
  • UX/UI Design
  • Enterprise Product Engineering
  • DevOps
  • Ongoing maintenance & Support (24x7)

The Challenge

The process of drug formulation involves many data points, and even the tiniest of details play a critical role in the development of the final product. It was crucial to ensure that the system was integrated with robust features and functionalities. These features guide the end-users through this entire process and enable a back-end validation engine to maintain a 100% accuracy in the formulation process.

A straightforward user interface and user experience were the critical components of this proposed product which would simplify the functionalities of the system. Hence, we focused on building an intuitive interface that will make this application easy to use for the end-users.

The Solution

Unified Infotech designed and engineered a sophisticated and secured Software-as-a-Service (SaaS) application that seamlessly enables end-users to develop new formulations supported by an intelligent recommendation engine. The application enables an end-to-end approval process by using a complete regulatory insight and Quality By Design (QBD) support for a smooth submission process.

The Result

The application was widely appreciated by the customers of the Client as it streamlined the process of drug formulation design, development and approval. Their clients were impressed by the seamless and intuitive user interface of the SaaS Application.