Achieve full QMS digitalization without the high costs of custom solutions. Quality Forward platform minimizes operational expenses with predictable updates and reduces validation efforts, ensuring scalability to support your business growth.
Quality Forward is a no-code platform offers out-of-the-box functionality while remaining highly configurable. This empowers Quality Assurance professionals to tailor workflows to evolving regulatory expectations without reliance on IT.
A trusted eQMS for industries where compliance and traceability matter every day. Built to meet FDA CFR, EU Annex 11, GxP, GMP, ISO, IEC, MDR, IATF & more, it helps teams maintain clean, reliable, inspection-ready quality operations.
Quality Forward eQMS aligns with global standards delivering end-to-end traceability across deviations, CAPAs, audits, and batch records. Automated workflows and centralized documentation ensure real-time audit readiness in even the most regulated environments.
Track and manage deviations effortlessly with automated real-time capture, customizable workflows, and integrated root cause analysis. Ensure compliance by linking deviations to CAPAs for continuous improvement. Instantly generate audit-ready reports to streamline regulatory inspections, keeping your processes efficient, transparent, and inspection-ready.
Manage CAPAs seamlessly with end-to-end tracking, automated reminders, and risk-based prioritization to address high-impact issues efficiently. Ensure proactive quality control with comprehensive documentation, maintaining full traceability from issue detection to closure. Stay compliant and streamline corrective actions with a system designed for efficiency and accountability.
Streamline complaint handling with a centralized platform for tracking and resolution. Automate response workflows to ensure timely follow-ups and corrective actions. Leverage trend analysis and reporting to identify recurring issues and enhance product quality. Maintain full regulatory compliance with complete documentation, ensuring audit readiness and seamless reporting.
Standardize and manage change approvals effortlessly with centralized requests, automated review cycles, and impact assessment tools. Evaluate risks and dependencies before implementation while ensuring compliance through version control. Streamline collaboration with stakeholders for faster approvals, keeping documentation accurate, up-to-date, and fully traceable.
Streamline audits with automated scheduling, tracking, and standardized checklists for consistency. Manage findings efficiently by assigning corrective actions and tracking progress in real time. Ensure regulatory compliance with comprehensive reporting aligned with FDA, ISO, and GMP standards. Maintain full audit readiness with a system designed for efficiency and accountability.
Streamline supplier qualification with centralized management, automated workflows, and risk-based ratings to ensure compliance and performance. Track approvals, onboarding, and re-evaluations seamlessly while maintaining full traceability with document and audit tracking. Keep supplier certifications, audits, and CAPAs organized for a more efficient, compliant, and transparent supply chain.
Proactively manage risks with structured assessment frameworks and custom scoring models to prioritize actions based on severity and impact. Track mitigation strategies effectively while ensuring compliance with industry standards. Align risk management with regulatory requirements for a streamlined, transparent approach to identifying, evaluating, and reducing potential risks.
Manage documents effortlessly with a secure, cloud-based repository for anytime access. Maintain compliance with automated versioning, ensuring controlled revisions. Customize user access controls to restrict or grant permissions based on roles. Keep a complete audit-ready log of edits and approvals for full regulatory traceability and streamlined compliance management.
Ensure staff compliance with automated, role-based training assignments and seamless SOP integration. Track progress, issue certifications, and maintain compliance-ready records for audits and inspections. Link training modules to relevant procedures to enhance understanding and efficiency, ensuring a well-trained workforce that meets regulatory standards with ease.
Capture safety incidents in real time with detailed logging and seamless root cause analysis. Link incidents to CAPAs for effective corrective actions while leveraging risk assessment tools to mitigate potential hazards. Ensure full compliance with industry safety standards through proactive tracking and documentation, keeping your workplace safe and audit-ready.
Our solution ensures regulatory reporting complTrack and manage deviations effortlessly with automated real-time capture, customizable workflows, and integrated root cause analysis. Ensure compliance by linking deviations to CAPAs for continuous improvement. Instantly generate audit-ready reports to streamline regulatory inspections, keeping your processes efficient, transparent, and inspection-ready.iance with ISO 13485 and FDA QSR, streamlines product lifecycle management, and enhances supplier and risk management to monitor performance and reduce compliance risks.
OurManage CAPAs seamlessly with end-to-end tracking, automated reminders, and risk-based prioritization to address high-impact issues efficiently. Ensure proactive quality control with comprehensive documentation, maintaining full traceability from issue detection to closure. Stay compliant and streamline corrective actions with a system designed for efficiency and accountability. solution ensures regulatory reporting compliance with ISO 13485 and FDA QSR, streamlines product lifecycle management, and enhances supplier and risk management to monitor performance and reduce compliance risks.
OuStreamline complaint handling with a centralized platform for tracking and resolution. Automate response workflows to ensure timely follow-ups and corrective actions. Leverage trend analysis and reporting to identify recurring issues and enhance product quality. Maintain full regulatory compliance with complete documentation, ensuring audit readiness and seamless reporting.r solution ensures regulatory reporting compliance with ISO 13485 and FDA QSR, streamlines product lifecycle management, and enhances supplier and risk management to monitor performance and reduce compliance risks.
Our solution ensures regulatory reporting compliaStandardize and manage change approvals effortlessly with centralized requests, automated review cycles, and impact assessment tools. Evaluate risks and dependencies before implementation while ensuring compliance through version control. Streamline collaboration with stakeholders for faster approvals, keeping documentation accurate, up-to-date, and fully traceable.nce with ISO 13485 and FDA QSR, streamlines product lifecycle management, and enhances supplier and risk management to monitor performance and reduce compliance risks.
Streamline audits with automated scheduling, tracking, and standardized checklists for consistency. Manage findings efficiently by assigning corrective actions and tracking progress in real time. Ensure regulatory compliance with comprehensive reporting aligned with FDA, ISO, and GMP standards. Maintain full audit readiness with a system designed for efficiency and accountability.
Streamline supplier qualification with centralized management, automated workflows, and risk-based ratings to ensure compliance and performance. Track approvals, onboarding, and re-evaluations seamlessly while maintaining full traceability with document and audit tracking. Keep supplier certifications, audits, and CAPAs organized for a more efficient, compliant, and transparent supply chain.
Proactively manage risks with structured assessment frameworks and custom scoring models to prioritize actions based on severity and impact. Track mitigation strategies effectively while ensuring compliance with industry standards. Align risk management with regulatory requirements for a streamlined, transparent approach to identifying, evaluating, and reducing potential risks.
Manage documents effortlessly with a secure, cloud-based repository for anytime access. Maintain compliance with automated versioning, ensuring controlled revisions. Customize user access controls to restrict or grant permissions based on roles. Keep a complete audit-ready log of edits and approvals for full regulatory traceability and streamlined compliance management.
Ensure staff compliance with automated, role-based training assignments and seamless SOP integration. Track progress, issue certifications, and maintain compliance-ready records for audits and inspections. Link training modules to relevant procedures to enhance understanding and efficiency, ensuring a well-trained workforce that meets regulatory standards with ease.
Capture safety incidents in real time with detailed logging and seamless root cause analysis. Link incidents to CAPAs for effective corrective actions while leveraging risk assessment tools to mitigate potential hazards. Ensure full compliance with industry safety standards through proactive tracking and documentation, keeping your workplace safe and audit-ready.
| ✔ Pharmaceuticals | ✔ Chemicals |
| ✔ Medical Device | ✔ Electronics |
| ✔ Biotechnology | ✔ Energy & Utilities |
| ✔ Food & Beverage | ✔ Mining, Oil & Gas |
| ✔ Automotive & OEM | ✔ Consumer Goods |
✔ Pharmaceuticals
✔ Medical Device
✔ Biotechnology
✔ Food & Beverage
✔ Automotive & OEM
✔ Chemicals
✔ Electronics
✔ Energy & Utilities
✔ Mining, Oil & Gas
✔ Consumer Goods
Configurable and No-Code
Design workflows that mirror industry-specific SOPs without writing code.
Cost-Effective and Scalable
Reduce overhead with a flexible cloud solution that adapts to pharma site or global rollouts.
Trusted by QA Leaders
Built for QA teams in highly regulated industries; life sciences, automotive, consumer goods manufacturing and more.
Seamless Integration
Connects with ERP, LIMS, MES, and EDMS systems to ensure data integrity and batch traceability.
AI-Powered Insights
Predict and prevent issues with AI-powered dashboards tracking deviations, CAPAs, and supplier risks.
We digitized our QI (CAPA/Containment) process with Quality Forward eQMS, replacing inefficient spreadsheets and rigid ITIL forms. The team helped us fully customize workflows, making the process far more efficient and user-friendly. Reporting is now easy, and we can generate custom client reports.
We implemented Quality Forward eQMS to replace several legacy eQMS solutions. The app's no code interface enabled us to meet all business requirements including automations and interfaces to other in house systems. Quality Forward's support during the process was exceptional supporting meeting timelines and budget with a smooth go live.
Great Product (intuitive, flexible) with great professional services who knew their subject very well (both the ServiceNow Platform and the QMS topic). Switching to the new system went really well, and everything is working smoothly.
Quality Forward has significantly improved our quality management processes. It centralized our documentation, streamlined our audits, and improved visibility across teams. Support has been responsive, and regular updates continue to add value.
MasterControl QMS has been around for years and is known for its depth, but that depth often comes with heavy projects, long change cycles, and high overhead. If you’re ready for a modern alternative that’s easier to change, faster to roll out, and runs on the ServiceNow platform your IT already trusts, Quality Forward is built to replace MasterControl without another multi-year QMS project.
Teams switch from MasterControl when every change feels like a mini-project. Quality Forward runs on ServiceNow and is fully no-code, so QA can adapt workflows without long vendor cycles.
Yes. You get a full eQMS like MasterControl QMS—CAPA, deviations, complaints, change control, audits, document control, training, supplier quality, risk—just delivered as ServiceNow apps instead of a heavy standalone stack.
Most customers go live in about 12–16 weeks, depending on scope and data. It’s a structured migration, not another multi-year MasterControl-style implementation.
Yes. We map your MasterControl objects and migrate records, attachments, and audit trails so you keep full traceability for inspections and regulators.
In many cases yes. With MasterControl you pay for a separate platform and complex upgrades. With Quality Forward you reuse ServiceNow, cut vendor overlap, and usually bring total cost of ownership down.
Yes. Quality Forward supports FDA 21 CFR Part 11, EU Annex 11, GMP, GxP, ISO 13485, ISO 9001 and more—built for life sciences and regulated manufacturing just like MasterControl.
Most don’t. If your teams already use ServiceNow, Quality Forward feels familiar on day one. They get a cleaner UI than MasterControl and stay in a platform they already know.
Instead of bolting MasterControl onto your stack, Quality Forward uses native ServiceNow integrations to connect with ERP, MES, LIMS, PLM, EDMS, HR and data lakes—less custom plumbing to maintain.
Yes. You can standardize global processes, support local variations, and manage all sites on a single ServiceNow instance, instead of juggling multiple MasterControl environments and projects.
You get an eQMS that changes as fast as your business: shorter release cycles, lower cost, one platform for IT and Quality, and no more feeling locked into a legacy MasterControl setup.
