

Automated Multi-Parameter Tablet Testing System
自动多参数片剂检测系统
- SKU TAA-0005
- Tablet Analysis
- CE (to be confirmed)
- IEC 61010-1 compliance (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Parameters measured | Weight, thickness, diameter, hardness |
|---|---|
| Throughput | about 10–30 tablets per minute |
| Weight range | 0–1000 mg with 0.1 mg resolution |
| Hardness range | 0–500 N |
| Dimension resolution | 0.01 mm |
| Friability module | Optional integrated drum |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <1216>, USP <1217>, USP <701>
What is the Automated Multi-Parameter Tablet Testing System?
An automated multi-parameter tablet testing system measures weight, thickness, diameter, hardness and sometimes friability in one sequence. It is chosen for high-volume release testing and process optimisation where statistics on many units are needed.
What is the Automated Multi-Parameter Tablet Testing System?
An automated multi-parameter tablet testing system measures weight, thickness, diameter, hardness and sometimes friability in one sequence. It is chosen for high-volume release testing and process optimisation where statistics on many units are needed.
Overview
The automated system feeds tablets from a hopper or tray onto a carousel that moves each unit through several stations. Weight is measured on a built-in balance, dimensions by a gauge or optical sensor, hardness by a motorised press, and friability by an integrated drum or a separate module. Results for every tablet are stored in software that reports mean, range, standard deviation and coefficient of variation, and can export data to a laboratory information management system. Because many units are tested, the system reveals trends within a batch that small manual samples may miss, which supports statistical process control and compression optimisation. Validation, calibration and data integrity features such as audit trails and user access control are essential in a GMP environment.
How does it work?
Tablet analysis applies mechanical and physical tests to individual dosage units. A hardness tester presses a tablet between two platens and records the force at which it breaks, expressed in newtons or kiloponds. A friability tester rotates tablets in a drum so they tumble and abrade, and the mass loss after a set number of revolutions indicates mechanical durability, normally less than one percent. A disintegration tester moves tablets up and down in a basket immersed in medium at 37 °C and records when no residue remains. A gauge measures thickness and diameter, and automated systems combine several tests so a batch is characterised unit by unit, which also supports statistical process control. Temperature, humidity, test speed and instrument calibration influence results.
What are the key features?
- Automatic feeding through multiple test stations
- Weight, dimensions, hardness and friability
- Per-tablet results with statistical reporting
- Export to LIMS and audit trail
- User access control for GMP compliance
- Trends within a batch for process control
What are the technical specifications?
A typical automated multi-parameter tablet testing system configuration offers parameters measured of Weight, thickness, diameter, hardness, throughput of about 10–30 tablets per minute, weight range of 0–1000 mg with 0.1 mg resolution, hardness range of 0–500 N, dimension resolution of 0.01 mm and friability module of Optional integrated drum. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Automated Multi-Parameter Tablet Testing System is used in high-volume batch release testing, compression process optimisation, statistical process control and contract tablet testing. Across the wider Tablet Analysis class, laboratories also deploy it for tablet hardness release testing, friability testing of tablets and disintegration testing of tablets and capsules.
Which standards and certifications apply?
Relevant standards and methods include USP <1216>, USP <1217>, USP <701>, Ph. Eur. 2.9.1, ICH Q2(R2) and IEC 61010-1. Certification candidates for this model are CE, IEC 61010-1 compliance and ISO 13485 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Keep the instruments in a room with controlled temperature and humidity, because tablets absorb or lose moisture and that changes hardness and friability. Condition samples before testing and record the conditioning time. Calibrate hardness load cells and verify disintegration temperatures at defined intervals, and check friability drums for wear. Clean residues from platens, baskets and drums, and inspect for corrosion from prolonged contact with water. Test adequate numbers of units, since tablet properties vary within a batch, and keep records of results, conditions and equipment status. For automated systems, back up data and review audit trails regularly.
How do I select the right Automated Multi-Parameter Tablet Testing System?
Specify an automated multi-parameter system when you test many batches, need statistics on large numbers of units, or want to optimise compression. Confirm which parameters are included, throughput, accuracy of each station, software data integrity and LIMS compatibility. Plan for calibration of multiple sensors and for regular maintenance.
How does it compare with other Tablet Analysis variants?
Choose instruments according to the tests in the pharmacopoeial monograph and the dosage form. Hardness, friability and disintegration testers are the core trio for conventional tablets, while thickness and diameter measurement supports weight and appearance control. Automated multi-parameter systems suit high-volume release testing and process optimisation, because they test many units and export statistics without manual records. Compare measurement ranges, accuracy and resolution, throughput, number of test positions or stations, and software for data handling and audit trails. For disintegration, check basket mesh size, stroke and temperature control; for friability, check drum dimensions, rotation speed and counting. Confirm calibration standards and qualification documents.
Full specifications
| Parameters measured | Weight, thickness, diameter, hardness |
|---|---|
| Throughput | about 10–30 tablets per minute |
| Weight range | 0–1000 mg with 0.1 mg resolution |
| Hardness range | 0–500 N |
| Dimension resolution | 0.01 mm |
| Friability module | Optional integrated drum |
| Software | Statistics, LIMS export, audit trail |
| Power supply | 220 V, 50 Hz, about 0.5 kW |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- High-volume batch release testing
- Compression process optimisation
- Statistical process control
- Contract tablet testing
Key features
- Automatic feeding through multiple test stations
- Weight, dimensions, hardness and friability
- Per-tablet results with statistical reporting
- Export to LIMS and audit trail
- User access control for GMP compliance
- Trends within a batch for process control
Frequently asked questions about Automated Multi-Parameter Tablet Testing System
Typically weight, thickness, diameter and hardness in one sequence, with friability available as an integrated or separate module. Some systems also measure disintegration time or carry out automated content uniformity sample preparation.
Tablet properties vary within a batch, and small samples may not reveal drift at the start or end of a compression run. Testing many units gives a clearer picture of variation and supports statistical process control and tighter specification setting.
User access levels, an audit trail with time stamps, electronic signatures where used, and export of raw data in a readable format. These support compliance with 21 CFR Part 11 and EU GMP Annex 11 expectations for electronic records.
Common physical tests are hardness or crushing strength, friability, disintegration time, thickness and diameter, and weight uniformity. Together with content uniformity and dissolution, they show that a batch will handle, package and release as intended.
For most compressed tablets the accepted limit is a mass loss of not more than one percent after 100 revolutions at 25 rpm, with no tablet cracked, broken or fragmented. The pharmacopoeial chapter defines the exact conditions and acceptance criteria.
Disintegration medium is held at 37 ±2 °C because higher temperatures speed disintegration and lower temperatures slow it, and results are compared against monograph limits measured under defined conditions. Temperature control and verification are therefore part of method validation.
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