

Tablet Friability Tester
片剂脆碎度仪
- SKU TAA-0002
- 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
| Drum internal diameter | about 286 mm |
|---|---|
| Drum depth | about 39 mm |
| Rotation speed | 25 ±1 rpm |
| Revolution count | 100 standard, programmable |
| Number of drums | 1 or 2 |
| Sample mass | about 6.5 g or per monograph |
By Lab Manufacturers China Technical TeamLast reviewed Standards: USP <1216>, USP <1217>, USP <701>
What is the Tablet Friability Tester?
A tablet friability tester tumbles tablets in a rotating drum and measures mass loss to assess mechanical durability. It is chosen to verify that tablets survive coating, packaging, transport and handling without chipping or breaking.
What is the Tablet Friability Tester?
A tablet friability tester tumbles tablets in a rotating drum and measures mass loss to assess mechanical durability. It is chosen to verify that tablets survive coating, packaging, transport and handling without chipping or breaking.
Overview
The friability tester uses a drum with an internal curved baffle that lifts and drops tablets as the drum rotates, usually at 25 rpm for 100 revolutions. Tablets are weighed before and after, and the percentage mass loss indicates abrasion and edge chipping. Most pharmacopoeial methods accept a loss of not more than one percent, with no tablet cracked, capped or broken, and a single drum is standard, though some instruments have two drums for parallel testing. A drum that is worn, scratched or fitted with the wrong baffle changes tumbling behaviour and results, so drums must be inspected and cleaned. Friability is especially important for tablets that will be film-coated or packed in blister packs and bottles, where mechanical stress is significant.
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?
- Rotating drum with internal curved baffle
- Standard speed of 25 rpm for 100 revolutions
- Mass loss reported as a percentage
- One or two drums for parallel testing
- Revolution counter with automatic stop
- Drum inspection for wear and damage
What are the technical specifications?
A typical tablet friability tester configuration offers drum internal diameter of about 286 mm, drum depth of about 39 mm, rotation speed of 25 ±1 rpm, revolution count of 100 standard, programmable, number of drums of 1 or 2 and sample mass of about 6.5 g or per monograph. 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 Tablet Friability Tester is used in tablet friability testing, coating process evaluation, packaging robustness assessment and formulation development. 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 Tablet Friability Tester?
Choose a friability tester with one or two drums and a clean, undamaged set of drums. Confirm rotation speed accuracy, revolution counting, drum dimensions and ease of cleaning. Pair it with a balance of sufficient resolution, since the result depends on accurate pre- and post-test weighing.
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
| Drum internal diameter | about 286 mm |
|---|---|
| Drum depth | about 39 mm |
| Rotation speed | 25 ±1 rpm |
| Revolution count | 100 standard, programmable |
| Number of drums | 1 or 2 |
| Sample mass | about 6.5 g or per monograph |
| Balance requirement | 0.001 g resolution |
| Power supply | 220 V, 50 Hz, about 0.1 kW |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Tablet friability testing
- Coating process evaluation
- Packaging robustness assessment
- Formulation development
Key features
- Rotating drum with internal curved baffle
- Standard speed of 25 rpm for 100 revolutions
- Mass loss reported as a percentage
- One or two drums for parallel testing
- Revolution counter with automatic stop
- Drum inspection for wear and damage
Frequently asked questions about Tablet Friability Tester
It measures the tendency of tablets to chip, abrade or break when tumbled, by the percentage of mass lost after a set number of revolutions. Low friability indicates tablets that survive coating, packaging and transport without losing material or appearance.
Often enough to give a sample mass of about 6.5 g, or a defined number of units as stated in the monograph, for example 10 tablets for larger tablets. The exact sample and acceptance criteria come from the pharmacopoeial chapter.
Scratches, dents or residual material change how tablets tumble and can cause extra abrasion or sticking. A clean, undamaged drum and the correct baffle ensure that the result reflects the tablet rather than the equipment.
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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