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Roll No
MPH-103T
M.Pharmacy (PCI), I Semester
Examination, December 2023
Modern Pharmaceutics
Time: Three Hours
Maximum Marks : 70
Note:
i) Attempt any five questions.
ii) All questions carry equal marks.
Write a detailed note on plant requirement, manufacturing and physiology of large volume Parenterals.
7Discuss preparation and evaluation of SMEDDS.
7Discuss in brief about the ICH and WHO for validation of equipments.
7What are the scope and advantages of validation in Pharmaceutical industry? How will you validate a solid dosage form at lab scale?
7Write a detailed note on concept of TQM.
7Give a detailed account on Inventory control and Production control management.
7Explain about Tablet compression theory.
7Describe different solubility enhancement techniques.
7Write a detailed note on F1 and F2 calculation with suitable examples.
7Describe dissolution and pharmacokinetics parameters.
7How will you determine the shelf life of liquid dosage form?
7What are the various stability testing protocols for Parenteral dosage form? Discuss.
7Write a detailed note on various optimization techniques.
7Distinguish between validation and calibration. What are the government regulation regarding validation?
7Write short note on (any two):
2×7-
a)
Contour design
-
b)
Manufacturing process models
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c)
Layout of tablet manufacturing plant
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d)
URS