DISSO III-7 release rate tester is suitable for USP apparatus 3 and USP apparatus 7 drug release rate testing. USP apparatus 3 is used for testing control-release drugs, enteric soluble drugs, soft gel, and chewable tablets. USP apparatus 7 is used for testing transdermal patches, implants, stents, stem and balloons. Features: 

• Switchable between USP apparatus 3 and USP apparatus 7 drug release rate testing
• Unique vessel covers design to prevent evaporation and media contamination
• Multiple sampling intervals and adjustable dip speed for flexible dissolution methods
• One-piece-molded clear water bath for easy observation
• Adjustable stroke length suitable for dissolution studies
• Data audit tracking function available and it complies to FDA 21 CFR Part 11 requirements

Extended functions:

• Capable of upgrading to an automated sampling system to increase efficiency
• Compatible with camera system to record drug release process
• DISSO III-7 is compatible with UV or HPLC. It can perform online dissolution analysis system
• Compatible with PERMETRO system to distinguish the permeation between generic drugs and original drugs, which can exist as a pre-BE study