Quality Management System
Quality
Quality Management System
Quality Control Management
At Healthcare Life Science Limited, we place the highest priority on quality, safety, and compliance across all our operations.
- Quality Assurance (QA): Ensures GMP compliance, conducts self-inspections, validates processes, implements CAPAs, and trains staff.
- Quality Control (QC): Tests raw materials, in-process samples, finished products, and reagents; manages batch release, stability studies, and documentation.
- Quality Compliance: Handles change controls, investigates deviations, manages complaints and recalls, and maintains audit-ready documentation.
- Quality Council: Reviews quality performance, assesses CAPAs, monitors improvement projects, and ensures strategic quality objectives are met.
- Continuous Improvement: Analyzes data, implements process enhancements, and adopts best practices to optimize quality and efficiency.
Our Commitment to Excellence
The Quality Control (QC) system at HPL ensures all materials and products meet required standards through testing, documentation, and monitoring. QC is responsible for sampling, specifications, analysis, and release procedures. Key responsibilities:
- Sampling, testing, and accepting/rejecting raw materials, packaging, intermediates, and finished products.
- Preparation and management of documentation, SOPs, analytical methods, certificates, and validation data.
- Monitoring product stability and participating in complaint investigations.
- Calibration and maintenance of analytical instruments and preparation of volumetric solutions.
- Ensuring proper training and certification of laboratory staff.
- Supporting Quality Assurance (QA) in batch review and release for distribution.
