Rigorous QA & QC Systems

Quality is not an act, but a habit. Our Quality Assurance (QA) and Quality Control (QC) departments operate independently, serving as the ultimate safeguard for every single product that leaves our facility.

Quality Assurance (QA) Overview

QA is embedded into every process, from raw material procurement to final product release. It’s the system that guarantees we are always operating under the prescribed Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). Our QA team conducts regular in-house audits and vendor qualifications.

Pharmaceutical Quality Assurance Documentation and SOP Checklist
  • Documentation Control: Comprehensive batch records, audit trails, and strict change control procedures.

  • Validation & Calibration: Strict schedules for all critical equipment, processes, and cleaning methods.

  • Training & Compliance: Continuous personnel training to ensure adherence to global regulatory standards.

Quality Control (QC) Laboratory

Our dedicated QC laboratory is equipped with state-of-the-art analytical instruments and staffed by highly skilled analysts. We perform exhaustive physical, chemical, and microbiological testing at every critical stage (Raw Material, In-Process, and Finished Product).

Key Analytical Protocols:

Pharmaceutical Quality Control laboratory with HPLC machine
  • High-Performance Liquid Chromatography (HPLC) for potency.

  • Gas Chromatography (GC) for purity and solvent residual analysis.

  • Fourier-Transform Infrared Spectroscopy (FTIR) for material identity.

  • Dissolution Rate Testing & Comprehensive Microbial Load Testing.

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