The Agilent one hundred automatic disintegration apparatus is a totally programmable solution that delivers reputable disintegration testing success. Our disintegration testing systems are compact and easy to handle, featuring precise temperature Manage and meeting regulatory compliance demands.
Disintegration test is arrives beneath 2nd classification that is qualitative test, to know the conduct with the drug products or can called it as being a physical test.
Our lab uses Practically completely Distek devices as They are really preferred from the laboratory analysts due to their reliability and ease of use."
The result of decades of innovation and working experience in the field of pharmaceutical testing, the DTGi Number of disintegration testers from Copley simplifies testing in R&D and QC environments.
We provide accredited electromagnetic compatibility expert services, serving to you to satisfy regulatory necessities, and improve the overall performance and protection of merchandise and gadgets as a result of our international laboratories.
Disintegration tests are having said that, helpful for examining the prospective value of formulation and procedure variables over the biopharmaceutical Houses on the tablet, and like a Command procedure to evaluate the quality reproducibility.
Conduct the calibration at time of set up and substitute for basket rack assembly According to Annexure -three working with vernier calipers or verify the compliance According to Sellers COA.
The disintegration test apparatus is usually a essential tool for guaranteeing the quality and performance of reliable oral dosage types, furnishing important details about their dissolution properties and bioavailability.
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Suspend the assembly within the beaker made up of the specified liquid and run the apparatus for the desired time. Take out the assembly from your liquid. The disintegrating tablets or capsules go the test if all of them have disintegrated.
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For changing the conventional basket to here special covered version for testing tough or comfortable gelatine capsules accepting to USP Chapter
The assembly is suspended in a very liquid medium in an appropriate vessel, preferably a one liter glass. The amount of liquid is this sort of that wire mesh in the organization The best place is no less than 25 mm below the floor in the liquid, and at a decreased level of a minimum of twenty five mm previously mentioned The underside on the glass.
Programmable capabilities—quick keypad interface directs impartial Charge of more info up to 3 separate test baskets. Baskets could be programmed to mechanically carry out from the beakers upon completion with the test