HPG Systems

The G 172 Digital Tablet Disintegration Test Apparatus is an advanced and precise instrument designed for the pharmaceutical industry to evaluate the disintegration time of tablets and capsules. This apparatus adheres to the stringent standards set by pharmacopoeias, ensuring that it provides reliable and reproducible results essential for quality control in drug formulation. Featuring a user-friendly digital interface, the G 172 allows for easy programming and monitoring of test parameters, including temperature control and timing, which are critical for accurate assessments. The apparatus is equipped with multiple test stations, enabling simultaneous testing of several samples, thereby enhancing productivity in laboratory settings. Its robust construction ensures durability, while the compact design allows for efficient use of laboratory space. With the G 172, pharmaceutical professionals can confidently assess the disintegration characteristics of their products, ensuring compliance with regulatory requirements and ultimately contributing to the safety and efficacy of medications.