The Agilent 100 automated disintegration apparatus is a fully programmable Remedy that provides trusted disintegration testing success. Our disintegration testing methods are compact and simple to control, showcasing specific temperature Handle and meeting regulatory compliance prerequisites.

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Temperature Manage—h2o bathtub temperature is controlled within the keypad, is usually achieved in minutes, and it is continuously exhibited to the front-facing LED panel

The holes coincide with Those people with the higher plastic plate along with the higher open up ends in the glass tubes. An appropriate suggests is presented to suspend the basket-rack assembly through the increasing and lowering product using a position on its axis.

Calibration procedure: Perform the calibration and history readings in the template as per Annexure -1.

Ans: Upward stroke in such a way that the wire mesh shall be beneath fifteen mm from the medium on the surface.

The Disintegration Test Apparatus shall encompass here basket rack assembly with a 1000m1 minimal sort beaker, for the immersion fluid, a thermostatic arrangement for heating the fluid among 35° and 39°C.

Assessing delayed release or enteric coated tablets the place samples must be immersed for specified amounts of time in numerous media

PD action in cables is calculated by attaching the break up-Main HFCT accessory around the cable earth ground. The outcomes are shown on the instrument in pico Coulombs (Computer system) as numerical values.

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At no time should the very best from the basket- rack assembly turn into submerged. Some time required for that upward stroke is equal to enough time required with the downward stroke as well as the transform in stroke route is really a clean changeover rather than an abrupt reversal of motion. The basket-rack assembly moves vertically together its axis.

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It is crucial to test your solutions to ensure they meet the regulatory demands; EMC certification is a compulsory need for numerous worldwide marketplaces.

Disintegration would be to be Executed to ascertain no matter whether tablets or capsules disintegrate within the prescribed time when positioned in a liquid medium with the experimental conditions.