Touchscreen Tablet Dissolution Test Apparatus VDA 8D (T)

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Touchscreen Tablet Dissolution Test Apparatus VDA 8D (T)

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MOQ : 1 Unit

Touchscreen Tablet Dissolution Test Apparatus VDA 8D (T) Specification

Noise Level
< 60 dB

Frequency
50 Hz

Features
Touchscreen control, Automated lift, Programmable test parameters, Audible alarms, High precision dissolution, Safety compliance

Phase
Single Phase

Temperature
Ambient to 45C (Heater Controlled)

Usage & Applications
Pharmaceutical Tablet & Capsule Dissolution Testing

Type
Other

Material
MS

Capacity
8 Vessels

Voltage
230V AC

Power
600 W (Approx.)

Weight (kg)
65 kg (Approx.)

Dimension (L*W*H)
1140 x 470 x 780 mm (Approx.)

Color
Silver/Grey with Clear Glass

Printer Connectivity
Available

Safety Features
Over-temperature protection, Low liquid level alarm

Number of Stirring Paddles/Baskets
8

Power Failure Recovery
Yes

Maintenance Feature
Self-diagnostic function

Sample Withdrawal
Automated Sampling (Optional)

Application Software
21 CFR Part 11 Compliant (Optional)

Stirring Speed Range
25 to 250 RPM (Adjustable)

Heater Type
Built-in Thermostatic Heater with Circulator

External Interface
RS232/USB

Validation
IQ/OQ/PQ Documentation Ready

Display
Large Color Touchscreen LCD

Language Support
Multilingual UI (Optional)

Vessel Volume
1000 ml (Standard)

USP Compliance
Complies with USP, IP, BP standards

Data Storage
Internal Memory / External USB

About Touchscreen Tablet Dissolution Test Apparatus VDA 8D (T)

Veego's latest Touch Screen based Tablet Dissolution Test Apparatus with advanced user features, PC connectivity, compatibility with our Auto Samplers.

Available in 8-station and 14-station models. Available with 21CFR, Part 11 Compliance as well.

Comprehensive Control and Automation

With its intuitive touchscreen digital control, programmable test parameters, and powerful data handling-both internally and via USB-the VDA 8D (T) ensures ease of operation. Automated lifting and optional automated sampling streamline workflow, while multilingual UI support guarantees accessibility, making it the optimal solution for efficient laboratory testing.

Precision, Safety, and Compliance

Certified for USP, IP, and BP standards, and with full IQ/OQ/PQ validation documentation available, this dissolution apparatus places a premium on precision and regulatory adherence. Features like over-temperature protection, low liquid level alarms, and power failure recovery maintain safety and integrity throughout the dissolution testing process.

FAQ's of Touchscreen Tablet Dissolution Test Apparatus VDA 8D (T):

Q: How does the touchscreen interface enhance the user experience for dissolution testing?

A: The large color touchscreen LCD interface provides intuitive navigation, allowing for easy setup of test parameters, monitoring of progress, and access to key functions. This enhances accuracy, minimizes manual errors, and streamlines the testing process for laboratory technicians.

Q: What is the benefit of having 8 stirring paddles/baskets in this apparatus?

A: With 8 stirring positions, the VDA 8D (T) can conduct multiple dissolution tests simultaneously, increasing throughput and efficiency in quality assurance laboratories for pharmaceutical tablets and capsules.

Q: When should I utilize the automated sampling option in this apparatus?

A: Automated sampling is beneficial during high-throughput testing or when precise, consistent sample withdrawal is needed. It minimizes manual intervention and ensures sample integrity at programmed intervals.

Q: Where can the data from the dissolution tests be stored or exported?

A: Test data can be stored on the instrument's internal memory or exported via external USB connectivity. Printer and RS232 connections also allow for direct report generation and integration with laboratory information systems.

Q: What process measures are in place to ensure safety during operation?

A: The VDA 8D (T) includes over-temperature protection, a low liquid level alarm, and power failure recovery, ensuring operator and sample safety throughout operation.

Q: How does the apparatus comply with international standards and validation requirements?

A: This apparatus is fully compliant with USP, IP, and BP standards, and is provided with IQ/OQ/PQ documentation for seamless validation. Optional application software ensures 21 CFR Part 11 compliance for data security and integrity.

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