The QMS
Quality Management System (QMS)
Ensure excellence and compliance across every stage of your operations with our advanced Quality Management System, designed specifically for the pharmaceutical industry. Our QMS streamlines document control, CAPA management, audits, training, and more, ensuring your processes meet the highest standards of quality and regulatory compliance.
Document Control
Centralized management of all critical documents, including SOPs, batch records, and quality manuals, with version control, approval workflows, and audit trails to ensure compliance and easy access.
Corrective and Preventive Actions Management
Streamlined workflows for identifying, documenting, and resolving issues, deviations, and non-conformances, ensuring that corrective and preventive measures are effectively implemented and tracked.
Audit Management
Comprehensive tools for planning, scheduling, conducting, and reporting on internal and external audits, with integrated findings tracking and CAPA linkage to address audit observations efficiently.
Change Control
A structured process for managing changes in processes, equipment, and documents, ensuring that all changes are assessed for risk, approved by the appropriate personnel, and implemented with full traceability.
Training Management
Robust tracking of employee training programs, certifications, and competency assessments, ensuring that staff are properly trained and compliant with regulatory requirements.
Risk Management
Tools for identifying, assessing, and mitigating risks across all areas of operations, aligned with ICH Q9 guidelines, to proactively manage potential quality and compliance issues.
QMS General Workflow
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Document Creation & Upload
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Training and Competency
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Process Execution and Monitoring
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Deviation and CAPA Management
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Audit Management
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Change Control
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Risk Management
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Continuous Improvement
