Trusted. Easily Configured. Cost Effective.
eQMS tailored for QA teams in Life Sciences and other highly regulated industries.
Simplify compliance, enhance product quality, and drive operational efficiency with AI capabilities.
Trusted. Easily Configured. Cost Effective.
eQMS tailored for QA teams in Life Sciences and other highly regulated industries.
Simplify compliance, enhance product quality, and drive operational efficiency with AI capabilities.
Easily Configured
For Your Needs
Built on ServiceNow, our eQMS ensures easy configuration, reducing validation efforts and cutting costs while maintaining compliance.
Cost-Effective and
Scalable
An eQMS that minimizes your operational costs with predictable updates, reducing validation efforts while ensuring scalability to support business growth.
Trusted by
Regulated Industries
A proven eQMS designed for compliance-driven sectors, backed by full audit trails, robust security, and adherence to global regulatory standards.
Our Key Processes in Quality Management
Deviations
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.
CAPA
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.
Complaint Management
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.
Change Control
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.
Audit Management
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.
Supplier Quality Management
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.
Risk Management
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.
Document Control
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.
Training 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.
Safety Incidents
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.
Equipment Management
Maintain equipment reliability while ensuring compliance with ISO, FDA, and GxP requirements. Automate quality workflows, reduce equipment-related risks, and drive operational excellence with a digital QMS designed for equipment management.
Our Key Processes in Quality Management
Deviations
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.
CAPA
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.
Complaint Management
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.
Change Control
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.
Audit Management
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.
Supplier Quality Management
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.
Risk Management
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.
Document Control
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.
Training 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.
Safety Incidents
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.
Equipment Management
Maintain equipment reliability while ensuring compliance with ISO, FDA, and GxP requirements. Automate quality workflows, reduce equipment-related risks, and drive operational excellence with a digital QMS designed for equipment management.
Tailored for Highly Regulated Industries
Quality Forward eQMS is designed to address the specific challenges faced by regulated industries, ensuring compliance, operational efficiency, and risk reduction.
Medical Device
Ensures ISO 13485 and FDA QSR compliance while streamlining product lifecycle, supplier, and risk management.
Pharmaceutical
Delivers GxP/21 CFR Part 11-aligned traceability for CAPAs, deviations, and batch records with automated audit-ready documentation.
Biotechnology
Uses AI for predictive quality and risk management, integrating with R&D and automating workforce compliance.
Food & Beverage
Enables HACCP and FSMA compliance with automated audit workflows and real-time ingredient quality tracking.
Electronics
Improves quality across complex supply chains with automated nonconformance, CAPA, and document control workflows.
Automotive & OEM
Supports IATF 16949 compliance with real-time tracking of deviations, audits, and supplier quality.
Chemicals
Facilitates GxP and EHS compliance by managing quality events, safety incidents, and documentation.
Energy & Utilities
Streamlines compliance with ISO and safety standards by centralizing quality processes and field data.
Mining, Oil & Gas
Enables safety and environmental compliance by digitizing incident reporting, inspections, and training management.
Consumer Goods
Supports fast-moving production with automated quality control, supplier oversight, and deviation management.
Why Quality Forward
Leading companies in Life Sciences and other highly regulated industries rely on Quality Forward to streamline quality management and maintain compliance. Join the organizations that have transformed their processes with this industry-proven solution.
Comprehensive Compliance Framework
Ensures consistency, accountability, and adherence to regulatory standards.
Enhanced Efficiency & Product Quality
Optimizes workflows to improve output with minimal rework.
Brand Protection & Risk Mitigation
Prevents quality issues and non-compliance to safeguard reputation.
Seamless Enterprise Integration
Connects teams, data, and processes for a unified approach to quality.
Operational Cost Reduction
Lowers expenses through automation, streamlined workflows, and smarter resource management.
Building Success Together with Strong Partnerships and Trust
