01.Q. Which
type of tablets are exempted from Disintegration testing?
02.Q.What are
the common variables in the manufacturing of tablets?
03. Q. Whether
bracketing & validation concept can be applied in process validation?
04. Q. What is
the difference between calibration and Validation?
05. Q. WHAT ARE
GOOD MANUFACTURING PRACTICES (GMP)?
06.Q. WHO
ENFORCES GOOD MANUFACTURING PRACTICES (GMP)?
07.Q.LIST OUT
THE APPEARANCE DEFECTS OF TABLES DURING COMPRESSION ACTIVITY ?
08.Q What is
the standard number of rotations used for friability test?
09.Q Which
capsule is bigger in size - size '0' or size '1'?
And For more questions and Answers
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