With its end-to-end data solution, eResidue Pro streamlines and centralizes all cleaning validation data, making it easier to track and analyze. Developed by Quascenta, eResidue Pro has a proven track record, with over 100 customers worldwide. It is the market leader in cleaning validation applications, having passed multiple regulatory inspections, including FDA, EMA, MHRA, and ANVISA.

Designed specifically for cleaning validation, eResidue Pro meets the requirements of GAMP5 and 21 CFR Part 11. It offers robust, pharma-specific solutions with features like a secure audit trail, role-based access, and electronic signature capabilities. eResidue Pro covers the entire cleaning validation lifecycle, from process design to ongoing monitoring, ensuring proactive compliance.

It provides automated workflows, built-in best practices, and seamless connectivity for efficient and effective quality compliance. With its modular and scalable design, eResidue Pro can be customized for different types of facilities, including Finished Drug Facilities, APIs, and Biotechs. It is a cloud-based application, accessible from anywhere, with zero software installation required.

eResidue Pro simplifies proof of compliance by keeping up with regulatory requirements, such as ANVISA, Health Canada, European Commission EudraLex, and more. It also incorporates inputs from industry guides and reports, ensuring a comprehensive solution. Ease of use and effortless reporting are key features of eResidue Pro.

It recommends a paperless workflow, with PDF reports available for immediate access. The application also offers powerful search and visualization capabilities, allowing quick insight into equipment and product data. With eResidue Pro, cleaning validation becomes easier, more efficient, and compliant, saving time and resources for pharmaceutical companies.

Schedule a demo today to experience the benefits of eResidue Pro firsthand