Quality Control Laboratory

Committed to Safety, Consistency, and Compliance in Pharmaceutical Manufacturing.

Quality control

Quality Control: Ensuring Excellence in Every Dose

Holden has a modern and well-equipped Quality Control Laboratory staffed by qualified professionals proficient in various fields such as pharmacy, chemistry, and microbiology.

The facility comprises separate chemical, instrumental, and microbiology laboratories, each furnished with state-of-the-art equipment including HPLCs, FTIR, UV-Visible spectrophotometers, Dissolution Test Apparatuses, stability chambers, and LAF units. These instruments undergo regular calibration to ensure accurate performance.

Analytical methods are routinely validated according to WHO and ICH Q2 guidelines, while product stability is assessed in accordance with ICH guidelines to ensure quality throughout shelf life.
Quality control procedures involve thorough testing of incoming materials like raw and packaging materials, intermediates, and finished products to verify compliance with specifications as per pharmacopeial standards and in-house parameters. Testing is performed using approved specifications and validated testing procedures.
Stringent document and data control measures within the quality control lab ensure data integrity and adherence to GLP (Good Laboratory Practice) standards.