Dissolution Test Apparatus
Dissolution testing is a critical quality control process in pharmaceuticals, assessing the rate of drug release from tablets or capsules under specific conditions. It ensures consistent effectiveness, aids formulation development, and verifies regulatory compliance for batch-to-batch consistency and therapeutic equivalence.
VDA-8D1
Microcontroller-based 8-station tester with high-res display, auto-sampler compatibility, versatile testing, and USP/IP/BP standards compliance for precise pharmaceutical dissolution analysis.
VDA-8D(ARM)
Upgraded version of the VDA-8D with enhanced features, including advanced microcontroller precision, making it an ideal choice for accurate and efficient dissolution testing.
VDA-8D(ARM) +VAS-S8
Powerful combination of microcontroller-based 8-station tester and auto-sampler with multi-syringe pump, ensuring unparalleled accuracy and flexibility.
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VDA-14D
Dual apparatus with 12+2 test stations, microcontroller precision, and compliance with IP/BP/USP standards, optimizing dissolution testing efficiency and accuracy.
VAS-S14
Precision-driven pairing of 8-station tester and auto-sampler with multi-syringe dosing pump, offering exceptional accuracy and efficiency.
Validation Kit
Comprehensive solution for mechanical validation of Dissolution Test Apparatus, including certification for assured accuracy and reliable performance in pharmaceutical quality control.