DS8000 & DS14000 Dissolution Test Apparatus – Precision, Compliance & Productivity for Modern Pharmaceutical Laboratories
DS8000 & DS14000 Dissolution Test Apparatus – Precision, Compliance & Productivity for Modern Pharmaceutical Laboratories
In today's pharmaceutical industry, dissolution testing is not just a regulatory requirement – it is a critical quality parameter that directly impacts product performance, bioavailability, and regulatory approval.
DS8000 Dissolution Test Apparatus – Reliable Performance for Routine Quality Control
The DS8000 is an 8-station dissolution system (6+2 configuration) designed for routine tablet and capsule testing in quality control laboratories. It offers the perfect balance between precision, flexibility, and cost-effectiveness.
Key Specifications – DS8000
- Configuration: 6+2 vessel configuration
- Apparatus Compatibility: USP Apparatus I (Basket) & II (Paddle)
- RPM Range: 20 – 350 RPM (programmable)
- Temperature Range: 20°C – 55°C with ±0.1°C accuracy
- Drive System: Microprocessor controlled
- Compliance: USP, BP, IP, EP | Data Integrity: 21 CFR Part 11
DS14000 Dissolution Test Apparatus – High-Throughput Efficiency for Advanced QC & R&D
The DS14000 offers expanded capability with a 14-station configuration (12+2). The dual 6+1 setup enables simultaneous testing of reference and test products, making it highly suitable for formulation development and bioequivalence studies.
Key Specifications – DS14000
- Configuration: 12+2 vessel configuration
- Apparatus Compatibility: USP Apparatus I & II
- RPM Range: 20 – 350 RPM (programmable)
- Sampling: Fully automated sampling with piston or syringe pump
- Software: 21 CFR Part 11 compliant with audit trail
Engineered for Regulatory Confidence
Both DS8000 and DS14000 systems are designed to meet international pharmacopeial standards including USP, BP, IP, and EP. Compliance features include precise RPM and temperature control, laser-marked components for traceability, IQ/OQ documentation support, and optional 21 CFR Part 11 software with secure audit trails.
Improve Productivity. Reduce Errors. Strengthen Compliance.
Automated configurations help reduce analyst dependency, improve reproducibility, minimize solvent consumption, enable unattended operation, and enhance overall laboratory efficiency – ensuring consistent, high-quality dissolution data.
Whether you need a compact 8-station system or a high-capacity 14-station automated platform, Labindia offers a solution tailored to your laboratory's needs. Request a product demonstration or speak with an application specialist today.