Dissolution Tester DT 950
Future‑ready digital dissolution tester for USP Methods 1, 2, 5 and 6.
DT 950 combines a 7‑inch touch interface with TestAssist guidance, integrated Audit Trail (21 CFR Part 11), Method and User Management, and flexible upgrade paths (6 to 8 stations, automatic tablet drop, per‑vessel temperature sensors) to deliver reliable, compliant testing and efficient workflows.
Key Features
- 100% USP/EP/JP compliant
- USP methods 1, 2, 5, and 6
- 7" touch interface with TestAssist guidance
- Upgradable at any time
- TestAssist wizard for easy step by step dissolution testing
- Automatic tablet drop
- High-head and low-head mode
- External Heater
- Integrated Audit Trail for full 21 CFR Part 11 compliance
- Method Management and User Management built in
- Upgradeable from 6 to 8 test stations
- Network/USB printing and FTP export for LIMS connectivity
Applications
Dissolution testing measures the extent and rate at which a dosage form (e.g., tablets, capsules, ointments) releases drug into solution — a key indicator for bioavailability, therapeutic effectiveness and manufacturing quality. Standardized procedures (USP General Chapter <711>) and qualified apparatus (basket, paddle, reciprocating cylinder, flow‑through cell) help ensure consistent product performance and regulatory compliance across production and R&D. DT 950 provides a robust platform for routine QC, method development and training use cases aligned with USP/EP/JP requirements.
