Disolutor

Our selection of Dissolution Tester instruments assists pharmaceutical laboratories, generic drug developers, and contract manufacturing plants in evaluating active ingredient release rates. Featuring 8-vessel and 12-vessel configurations compatible with USP Apparatus 1 baskets and Apparatus 2 paddles, these units maintain precise water bath temperature regulation and automated sampling in compliance with USP <711> and EP 2.9.3 monographs.

Equipped with electronic audit logging and user access controls for FDA 21 CFR Part 11 requirements, this dissolution tester category supports both early formulation development and routine batch release. Integrating these automated dissolution testing systems into your quality verification routines streamlines sample handling and delivers dependable release rate data across solid dosage forms.