USP Dissolution Method Validation Testing
The USP Dissolution Method Validation Testing is a critical service in pharmaceutical quality assurance. This process involves ensuring that drugs are released from their dosage forms according to the specifications outlined in the United States Pharmacopeia (USP). Dissolution testing evaluates drug product performance by measuring the rate and extent of dissolution, which directly impacts bioavailability and patient safety.
Dissolution testing is performed using various apparatuses such as桨Ș<|im_start|>⚗ yans
