Tablet Disintegration Tester
Determines the time a tablet or capsule takes to break apart under defined conditions.
Raises and lowers a basket-rack of tablets in a heated liquid and records the time at which no residue remains on the mesh. It answers a simpler question than dissolution — whether the dosage form breaks up at all — and is the release test wherever a dissolution method is not required.
- Import, delivery and installation
- IQ/OQ and calibration by our Technical Services Division
- Genuine spares and operator training in Dhaka
Specifications
Specifications vary by model and configuration — the brochure carries the full range. Tell us your throughput, sample type and compliance requirement and we will confirm which model fits.
Download the brochure (PDF · 4 KB)Compliance & qualification
Disintegration is described in USP <701> and Ph. Eur. 2.9.1.
Applications
Release testing of uncoated, coated and enteric tablets and capsules; formulation screening.
Also in Pharmaceutical Testing & Analytical Solutions