Dissolution Tester

Dissolution Tester

This is a precision laboratory instrument used to measure the rate and extent at which active pharmaceutical ingredients (APIs) are released from tablets or capsules into a dissolution medium. This test is critical for evaluating drug release behavior, bioavailability, and in-vitro performance of oral solid dosage forms.

The instrument accurately simulates physiological conditions to generate reliable and reproducible dissolution profiles, making it an essential system for pharmaceutical quality control and research laboratories.

Use & Standards

• Used for dissolution testing of tablets and capsules
• Designed in accordance with USP, BP, and IP pharmacopeial requirements
• Meets ICH guidelines for dissolution, stability, and quality studies

Laboratory Benefits

Supports regulatory submissions and QC validation
Provides accurate drug release profiles for solid oral dosage forms
Essential for bioequivalence and stability testing
Ensures batch-to-batch consistency and product reliability