Quality Assurance & Quality Control

quality is not a department—it is our core identity. We operate on the principle that every dose we manufacture carries a promise of safety and efficacy.

Quality Assurance & Quality Control

At Air Pharma, quality is not a department—it is our core identity. We operate on the principle that every dose we manufacture carries a promise of safety and efficacy.

Quality Control (QC)

Our QC laboratories are equipped with high-precision analytical instrumentation to monitor the chemical and physical integrity of our products at every stage.

  • Raw Material Testing: Comprehensive analysis of APIs (Active Pharmaceutical Ingredients) and excipients before they enter the production floor.
  • Advanced Instrumentation: Utilization of High-Performance Liquid Chromatography (HPLC), UV-Visible Spectroscopy, and Dissolution Testing to ensure batch-to-batch consistency.
  • Stability Studies: Dedicated stability chambers maintaining Zone IVb conditions to ensure products remain effective in Pakistan’s unique climate.
  • Microbiological Testing: Rigorous monitoring of water purity and environmental microbial counts to ensure a sterile manufacturing environment.

Quality Assurance (QA)

Our QA team oversees the entire lifecycle of a product, ensuring that every process follows the strict guidelines of cGMP and DRAP.

  • Document Control: Maintaining meticulous Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) for total traceability.
  • In-Process Quality Control (IPQC): Real-time monitoring of tablet hardness, friability, weight variation, and liquid viscosity during actual production.
  • Validation & Qualification: Regular calibration of machinery and validation of cleaning processes to prevent cross-contamination.
  • Self-Inspection: Periodic internal audits to ensure our facility stays ahead of international pharmaceutical standards and regulatory requirements.
100% DRAP Compliance | cGMP Certified | BP/USP Standards Adherence 
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