APAS
Automatic Preparation of Analytical Sample
The complete automation solution for pharmaceutical QC laboratories. APAS combines multiple FMAP modules into a cohesive system that automates your entire sample preparation workflow.
Automated Workflow
From sample loading to analysis-ready output, APAS handles every step with precision and full traceability.
Weighing
Samples weighed with 0.1mg precision using integrated analytical balance.
Liquid Dosing
Solvents added with ±0.1ml accuracy via time-pressure dispensing method.
Homogenizing
Ultrasonic bath (40kHz) and vortex mixing for complete dissolution.
Temperature Control
Peltier cooling system maintains 10-60°C for sensitive samples.
Extraction
Liquid extraction with integrated filtration using 55-filter buffer.
Output
Analysis-ready samples in 15ml or 50ml centrifuge tubes.
See APAS in Action
Watch how APAS automates the complete sample preparation workflow. From weighing to final aliquoting, see the precision and efficiency that transforms laboratory operations.
- Unattended operation for routine sample preparation
- Real-time monitoring and status updates
- Complete audit trail for every sample
Applications
APAS is designed for the most common pharmaceutical QC sample preparation workflows.
Dissolution Testing
Automate sample preparation for USP dissolution testing protocols.
Content Uniformity
Precise sample preparation for tablet content uniformity testing.
Stability Studies
Consistent sample preparation across long-term stability programs.
Raw Material Testing
Efficient preparation of incoming raw material samples.
Transform Your Sample Preparation
See how APAS can improve efficiency, reduce errors, and ensure compliance in your QC laboratory.
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