A Review Of tablet disintegration test apparatus
A Review Of tablet disintegration test apparatus
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The Agilent 100 automated disintegration apparatus is a completely programmable Remedy that provides trusted disintegration testing success. Our disintegration testing programs are compact and easy to deal with, that includes exact temperature Command and Assembly regulatory compliance necessities.
This SOP is relevant for Procedure and calibration of disintegration test apparatus (Electrolab make), that will be employed for locating disintegration time of capsules or tablets in top quality Regulate Division.
To cope with these variables, the UltraTEV Plus2 has the aptitude to implement various measurement techniques and employ A variety of sensors to permit extensive testing of various assets and detection of PD.
Document the looking at in calibration structure following interval According to calibration format, repeat a similar procedure for remaining aspect jar and report the observation in calibration format.
The design on the basket-rack assembly can be relatively various offered specs for that glass tubes, along with the monitor mesh sizes are unchanged.
Tinius Olsen manufactures various substantial capability pendulum effects testers, a lot of which may be very easily improved from a Charpy to an Izod configuration or even into a tensile impact configuration.
The time taken for the tablet or capsule to disintegrate into small particles is recorded. The disintegration time of the tablet or capsule need to comply with the pharmacopeial specifications to make certain that the drug solution is of good quality.
Our community of laboratories supports you with testing plans that supply a complete choice of certification and validation providers to fulfill your distinctive testing desires.
PROCEDURE:- Location a single dosage unit in Every single on the six tubes with the basket and when specified add a disc. Run the apparatus applying water because the immersion fluid Until A further liquid is specified and retain its temperature at 35–39 °C. At the end of the specified time lift the basket through the fluid and observe the dosage units, all the dosage models have disintegrated entirely.
Ph. Eur. and USP and compliant Integrated, precision temperature Regulate and measurement Solitary-stage Digital temperature calibration Intuitive touchscreen Handle to simplify Procedure 1 to 4 test station unit configurations, in addition independent station Management unit option click here Considerable facts reporting output solutions: RS 232, USB A and USB B Adjustable stroke frequency Management for accelerated or substantial sensitivity testing Choice to automate and remotely Command DTGi programs
The latest version in the ACFM combines the condition-of-the-artwork accuracy and simplicity of use that the original ACFM introduced to the market with a simplified interface and more compact offer.
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As per Indian Pharmacopeia the quantity with the liquid is this sort of which the wire mesh at its optimum stage is at the least twenty five mm underneath the area in the liquid and its decreased position is at the least twenty five mm above the bottom of beaker.
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