Introduction
Trust E 8 GEN 2 basic is an 8-station dissolution tester for pharmaceutical labs. It complies with USP, IP, and Ph. Eur. specifications. This system is designed for reliable and repeatable testing. The Trust E 8 GEN 2 basic features a 7-inch touch screen and advanced compliance capabilities.
Product Overview
This 8-station dissolution tester is built for modern quality control environments. It operates on a robust software platform that ensures full 21 CFR Part 11 compliance. This includes features like fingerprint login, a detailed audit trail, and e-signatures. The instrument is designed for ease of use with a motorized lift and precise vessel centering. The unique TimeAction™ function allows for programmed media changeovers, making this dissolution tester suitable for sustained and controlled-release products.
Key Features
- 8-Station Capacity: Allows for simultaneous testing of up to 8 samples.
- 21 CFR Part 11 Compliant: Includes fingerprint login, audit trail, and e-signatures.
- 7-inch Touch Screen: Provides an intuitive interface for programming and monitoring.
- USP Compliance: Supports methods for USP Apparatus 1, 2, 5, and 6.
- Motorized Lift Mechanism: Ensures smooth, vibration-free movement of the stirrer head.
- TimeAction™ Function: Enables programmed media changeovers for complex dissolution profiles.
Technical Specifications
| Model | TrustE-08 Basic (Gen-2) |
| No. of stations | 8 |
| Speed range | 20 to 300 RPM |
| Speed accuracy | ±0.5 RPM |
| Temperature range | 20°C to 40°C |
| Temperature accuracy | ±0.1°C |
| Display | 7″ TFT touch screen |
| Report Storage | Up to 50000 |
| Dimensions (W x L x H) | 517 x 712 x 690 mm |
Applications
- Quality control testing of solid dosage forms.
- Dissolution profiling of immediate and extended-release drugs.
- Methods requiring USP 1 (Basket), 2 (Paddle), 5 (Paddle over Disk), and 6 (Rotating Cylinder).
- Laboratories requiring 21 CFR Part 11 data integrity.
Pricing
Please contact us for consultation and detailed quotation.
Frequently Asked Questions (FAQ)
1. What is the Trust E 8 GEN 2 basic used for?
It performs USP-compliant dissolution tests for up to 8 samples. It is ideal for QC and R&D labs requiring data integrity.
2. Does this dissolution tester meet 21 CFR Part 11 requirements?
Yes, it offers full 21 CFR Part 11 compliance features. This includes fingerprint login, audit trails, and e-signatures.
3. What USP methods does this tester support?
It supports USP Apparatus 1 (Basket), 2 (Paddle), 5 (Paddle over Disk), and 6 (Rotating Cylinder).
4. What is the TimeAction™ function?
This function allows for programmed, automatic media changes. It is useful for mimicking the GI tract for extended-release drugs.
5. Is this model suitable for automated sampling?
No, this is a standalone tester designed for manual sampling.
Conclusion
The Trust E 8 GEN 2 basic is a robust solution for modern pharmaceutical labs. It combines an 8-station capacity with full 21 CFR Part 11 compliance features. This ensures reliable and traceable results for dissolution testing. Contact us for more information.
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