Tablet Compression - In process checks in Pharmaceutical industry l Interview Question and answers

Compression - In process checks in Pharmaceutical industry l Disintegration test l Friability l Interview Question and answers
-----------------------------------------------------------------------------------------------
Pick your favourite topic video from below playlist:
1. QMS - Quality Management System in Pharmaceutical industry : • QMS - Quality Manageme...
2. QA- Quality assurance in Pharmaceutical industry. : • QA- Quality assurance ...
3. QC - Quality Control in Pharmaceutical industry :
• QC - Quality Control i...
4. OSD - Tablet Manufacturing in Pharmaceutical industry :
• OSD - Tablet Manufactu...
5. Injectable processing - Injectable processing or Sterile dosage formulation : • Injectable processing ...
-----------------------------------------------------------------------------------------------
Questions covered:
Q. What are the important in-process checks performed during tablet compression process ?
Q: Which USP chapters are referred for compression in-process checks ?
Q. What should be the frequency for in-process checks done during compression process ?
Q. What is the purpose of in-process checks during tablet compression ?
Q. What is the purpose of the disintegration test in tablet compression process ?
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. What is the purpose of the Friability test in pharmaceutical industry ?
Q. For how many rotations we should rotate friability test apparats and at what RPM ?
Q. How many tablets we should take for friability test?
Q. Describe the procedure for conducting a friability test on tablets ?
Q. Why dedusting is important prior to friability test?
Q. What is formula for calculating friability and what is acceptance criteria ?
Q. Which units are commonly used for measuring tablets hardness ?
Q. Which defects can be identified during visual inspection of compressed tablets ?
Q. How many tablets shall be considered during initial setting of compression machine for weight variation testing ?
Q. What is weight variation limit as per USP?
Q. What is the operating principle of a metal detector used in tablet compression ?
Q. Why is it essential to monitor compression force during tablet production ?
Q. With what pieces metal detector is challenged ?
Q. What is evaluated during tablet dissolution testing ?
Q. What is relation between tablet thickness and tablet hardness during tablet compression process ?
Q. What should be the action plan taken in case we miss the in-process test frequency or out of limit result observed ?
-----------------------------------------------------------------------------------------------
Keywords to find this video:
friability test interview questions,friability question and answer,friability test,disintegration test,compression interview question and answers,pharmaceutical industry,granulation process in pharmaceutical industry,pharmaceutical interview questions and ansewrs,friability test interview questions in hindi,most important interview questions and answers in pharmaceutical industry,friability test procedure,disintegration test for tablets
-----------------------------------------------------------------------------------------------
Copyright disclaimer:
“Any illegal reproduction of this content will result in immediate legal action.”