Microprocessor Dissolution Test Apparatus is a solid state instrument designed for the determination of active drug ingredient in any pharmaceutical formulation, tablet or capsule as per IP and USP specifications. This apparatus evaluates adequate bio-availability and provides necessary information to formulate in the development of therapeutically optimum dosage forms. The instrument is designed and manufactured for pharmaceutical industries. It is used in quality control and R & D to determine compliance with the dissolution requirement of the Tablet and Capsule as per USP/IP standards.

Instrument uses the latest microprocessor technology and advanced engineering techniques so as to give enhanced accuracy and reproducibility. The system has user friendly prompts, which guide you throughout the measurement process.

System is equipped with 4 line alphanumeric LCD display with backlit and 19 soft touch membrane type keys that provides a convenient interface for entering the data. Independent stirrer and platform keys on the front panel allow the user to easily start/stop stirrer movement or displacement of platform in the required direction at any time.

Features:

• 14 Station (Model – 2914)
• 12 Station (Model – 2912)
• Complies with USP, IP specifications
• Extremely useful for pharmaceutical labs
• Programmable stirrer control (25 to 200 RPM)
• 20 x 4 line alphanumeric LCD display with backlit
• 19 Soft touch membrane type keys
• 20 independent programmable setups for routine & sustain mode with storage
• 200 sample storage facility
• Printer attachment facility
• Audio visual indicators for system status
• Easy to empty and clean water bath with bottom drainage
• Continuation of last sample run in case of power failure

LED’s: 4 LED’s for different status indications. 3 LED’s for test status like Run, Alarm, End & 1 LED for heater ON/OFF status

Microprocessor Dissolution Test Apparatus is a solid state instrument designed for the determination of active drug ingredient in any pharmaceutical formulation, tablet or capsule as per IP and USP specifications. This apparatus evaluates adequate bio-availability and provides necessary information to formulate in the development of therapeutically optimum dosage forms. The instrument is designed and manufactured for pharmaceutical industries. It is used in quality control and R & D to determine compliance with the dissolution requirement of the Tablet and Capsule as per USP/IP standards.

Instrument uses the latest microprocessor technology and advanced engineering techniques so as to give enhanced accuracy and reproducibility. The system has user friendly prompts, which guide you throughout the measurement process.

System is equipped with 4 line alphanumeric LCD display with backlit and 19 soft touch membrane type keys that provides a convenient interface for entering the data. Independent stirrer and platform keys on the front panel allow the user to easily start/stop stirrer movement or displacement of platform in the required direction at any time.

Features:

• 14 Station (Model – 2914)
• 12 Station (Model – 2912)
• Complies with USP, IP specifications
• Extremely useful for pharmaceutical labs
• Programmable stirrer control (25 to 200 RPM)
• 20 x 4 line alphanumeric LCD display with backlit
• 19 Soft touch membrane type keys
• 20 independent programmable setups for routine & sustain mode with storage
• 200 sample storage facility
• Printer attachment facility
• Audio visual indicators for system status
• Easy to empty and clean water bath with bottom drainage
• Continuation of last sample run in case of power failure

LED’s: 4 LED’s for different status indications. 3 LED’s for test status like Run, Alarm, End & 1 LED for heater ON/OFF status