Manual disintegration testing for pharmaceuticals
In pharmaceutical environments, ensuring that tablets disintegrate within defined timeframes is critical for quality control and compliance. Accurate disintegration testing helps prevent issues like incomplete dissolution and inconsistent medication delivery, maintaining high standards for patient care and product performance.
Perform reliable disintegration tests with precision
The ZT 121 light, from ERWEKA, is designed for precise manual disintegration testing, compliant with USP, EP, and JP standards. This compact unit features a flow-through heater and a moulded PET water bath, ensuring no leaks and easy cleaning. It is operated via a user-friendly membrane keypad, allowing you to enter and monitor parameters such as run time and water bath temperature on bright LED displays. The device starts counting run-time automatically when the basket rack is lowered, making it a highly efficient tool for quality control. With options that include IQ/OQ/PV qualification documents and water stabilizers, the ZT 121 light provides flexibility and reliability in pharmaceutical disintegration testing.
Benefits
- Ensures compliance with USP, EP, and JP standards
- User-friendly interface with membrane keypad and LED displays
- Compact design with easy-to-clean PET water bath
- Automatic run-time counting for efficiency
- Optional qualification documents and water stabilizers available