Drug samples are stored under accelerated, intermediate, or real-time (long-term) conditions inside stability chambers.

Samples of drug products or raw materials are prepared and subjected to analytical techniques to detect, quantify, and classify residual solvents.

Product samples are aseptically transferred into sterile culture media and incubated under controlled conditions to promote the growth of any contaminating microorganisms.

Potency tests evaluate a drug’s ability to produce a specific biological response by comparing its activity against a known reference standard.

Samples are inoculated into or onto selective culture media and incubated under controlled conditions to encourage the growth of bacteria and fungi (yeasts and molds).

The dosage form is placed in a disintegration test apparatus containing a prescribed liquid (typically water, simulated gastric, or intestinal fluid) and maintained at body temperature (37°C ± 2°C).

The dosage form is placed in a dissolution vessel containing simulated gastric or intestinal fluid, and agitated using a USP Dissolution Apparatus

Samples are digested or treated with appropriate acids/solvents and analyzed using advanced instrumentation to determine heavy metal concentrations with high sensitivity and accuracy.

Prepared samples are measured using a calibrated pH meter, with test conditions depending on the specific dosage form.

Biological samples are stored under controlled temperature, humidity, and light conditions, and tested at scheduled intervals for physicochemical, biological,

Samples are analyzed by measuring the loss of weight upon drying using either conventional oven-drying methods or advanced moisture analyzers.