Streamline GxP compliance and batch release with a cloud-native QMS for Pharmaceuticals, built to reduce risk and boost efficiency for pharma teams.
Streamline GxP compliance and batch release with a cloud-native QMS for Pharmaceuticals, built to reduce risk and boost efficiency for pharma teams.
Operating under constant regulatory scrutiny, pharmaceutical manufacturing demands robust systems that prevent compliance failures, reduce batch release delays, and ensure product integrity. Quality Forward supports inspection readiness by digitizing and integrating every critical quality process.
Ensure suppliers meet GMP and material quality standards. Digitize supplier onboarding, audits, risk profiles, and certifications with end-to-end traceability.
Identify and mitigate formulation, equipment, or supply risks using configurable frameworks and severity-based scoring models. Stay ahead of compliance threats.
Ensure role-based qualification with automated training assignments, completion tracking, and real-time audit readiness.
Be inspection-ready at all times with structured audit scheduling, response workflows, and secure audit documentation.
Capture deviations and quality events at the point of occurrence. Trigger immediate investigations and track resolution for trend analysis.
Investigate and resolve product complaints efficiently with centralized documentation, root cause analysis, and automated workflows.
Digitize all SOPs, batch records, validation protocols, and regulatory filings. Ensure compliance with FDA 21 CFR Part 11 and GMP documentation standards.
Enforce structured workflows for process, equipment, and material changes. Assess, approve, and implement changes with full compliance to ICH Q10.
Initiate CAPAs directly from deviations, audits, or complaints. Monitor effectiveness checks and align remediation activities with risk priority.
Capture and manage batch deviations and non-conformances in real time. Ensure containment, impact assessment, and compliance-based resolution.
Pharmaceutical manufacturing demands precision, traceability, and compliance at every stage, this is where Quality Forward comes in to unify deviations, CAPAs, change control, and batch records in a single validated platform – purpose-built for GMP environments.
Streamline quality events, reduce cycle times, and ensure inspection readiness with full visibility across global operations; all powered by the trusted Now Platform.
Design workflows that mirror pharma-specific SOPs without writing code.
Reduce overhead with a flexible cloud solution that adapts to pharma site or global rollouts.
Built for QA teams at top pharmaceutical manufacturers maintaining global GMP compliance.
Connects with ERP, LIMS, MES, and EDMS systems to ensure data integrity and batch traceability.
Predict and prevent issues with AI-powered dashboards tracking deviations, CAPAs, and supplier risks.
Secure, validated, and ready for enterprise deployment on the ServiceNow platform.
