Pro-DRE streamlines the data review process across various GxP systems, including CDS, FTIR, UV, KF, LIMS, and MES. By automating repetitive tasks and flagging exceptions, Pro-DRE enhances compliance and productivity, allowing users to focus on core activities with confidence.

Problem Statement/Industry Need:

In the pharmaceutical industry, ensuring data integrity and compliance with regulatory standards is paramount. However, manual data review processes across various GxP systems are time-consuming, prone to errors, and hinder productivity. Pharmaceutical companies face challenges in efficiently managing data review tasks, leading to potential delays in product development and regulatory submissions.


Pro-DRE offers an automated solution to streamline the data review process across multiple GxP systems. Leveraging advanced algorithms and Process Automation Tools, Pro-DRE automates repetitive tasks such as data verification, anomaly detection, and exception handling. By integrating with existing systems, Pro-DRE identifies discrepancies and deviations in real-time, enabling proactive intervention and ensuring data integrity throughout the product lifecycle.

Business Application:

Pharmaceutical companies can leverage Pro-DRE to enhance compliance, productivity, and efficiency in data review processes. By automating routine tasks, Pro-DRE allows scientists and regulatory teams to focus on high-value activities such as data analysis and decision-making. Additionally, Pro-DRE facilitates faster review cycles, accelerating time-to-market for new products and reducing regulatory risk. With Pro-DRE, pharmaceutical companies can improve operational agility and maintain a competitive edge in the market.

reduction in cycle time
improvement in Productivity

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