Quality Forward is a cloud-based (SaaS) eQMS built on the ServiceNow platform, designed for highly regulated industries such as life sciences, automotive, consumer goods and more. It centralizes and automates quality processes to support compliance with global standards like FDA 21 CFR Part 11, EU MDR, ISO 13485, and GxP.
The platform includes built-in validation, audit trail, electronic signatures, and automated workflows that align with FDA, EMA, ISO, and ICH standards. It supports real-time traceability, centralized documentation, and role-based access for full compliance oversight.
Yes. Quality Forward offers a true no-code configuration engine. QA teams can tailor forms, workflows, approval paths, and dashboards without IT support -ideal for adapting quickly to evolving SOPs or regulatory changes.
Quality Forward out of the box processes are listed below: Additional processes can be easily configured.
Yes. The eQMS supports full API integration with ERP, MES, LIMS, CRM, HRIS, and any other system with Open APIensuring data integrity and minimizing manual entry.
Quality Forward includes a full validation package (IQ/OQ/PQ), complete with auto-executable scripts. The system supports Part 11–compliant eSignatures and audit trails, making it inspection-ready by design.
The platform is trusted by QA teams across pharmaceutical manufacturers, medical device companies, biotech firms, and other regulated companiesranging from startups to global enterprises.
Deployments are fast and cloud-native. With pre-configured templates and no-code configuration, most implementations are completed in weeks, not months.
Quality Forward supports multi-site operations with centralized oversight, role-based access by region or site, and support for global regulations. It’s built to scale with your business – whether you’re operating one facility or a global network.
Unlike legacy or low-code systems, Quality Forward delivers:
Quality Forward is an eQMS application built on the ServiceNow platform. It extends the platform’s value into regulated environments by enabling end-to-end Quality Management across pharmaceuticals, medical devices, biotech, and other regulated industries. The solution delivers the structure, traceability, and compliance that QA teams require, without compromising speed or usability.
Quality Forward supports compliance-driven industries including:
With pre-validated workflows, no-code configuration, and fast time-to-value (4–8 weeks), Quality Forward allows clients to go live quickly, without extensive development or regulatory overhead. QA teams benefit from a scalable, ready-to-use system that supports compliance from day one.
