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Disintegration test in Pharmaceutical industry l Tablet / Capsule disintegration time 25 Interview Question
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Questions covered:
Q. What is the purpose of the disintegration test in pharmaceuticals?
Q. Explain the difference between disintegration and dissolution testing?
Q. Can you describe the apparatus used in the disintegration test, and how does it function?
Q. What are the key parameters or values as per USP Chapter No.701 for disintegration test?
Q. How is the disintegration test performed, and what are the key steps involved?
Q. Which USP chapter talk about disintegration test and what is title of that chapter?
Q. What is disintegration time?
Q. Why we need to check disintegration time of tablet or capsule during manufacturing?
Q. What is L1 and L2 stage disintegration test?
Q. Why we put ‘Disk’ over tablet / capsule during disintegration test ?
Q. Which are the most commonly used disintegrating agents in the Tablet formulation ?
Q. Which Granulation stage parameters affect on disintegration time ?
Q. Which Compression stage parameters affect on disintegration time ?
Q. Which Media is commonly used as a Media for disintegration test ?
Q. When we should perform tablet disintegration test during tablet compression stage ?
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