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Total No. of Questions: 8
Total No. of Printed Pages: 2
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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.

1. a)

Write a detailed note on plant requirement, manufacturing and physiology of large volume Parenterals.

7
b)

Discuss preparation and evaluation of SMEDDS.

7
2. a)

Discuss in brief about the ICH and WHO for validation of equipments.

7
b)

What are the scope and advantages of validation in Pharmaceutical industry? How will you validate a solid dosage form at lab scale?

7
3. a)

Write a detailed note on concept of TQM.

7
b)

Give a detailed account on Inventory control and Production control management.

7
4. a)

Explain about Tablet compression theory.

7
b)

Describe different solubility enhancement techniques.

7
5. a)

Write a detailed note on F1 and F2 calculation with suitable examples.

7
b)

Describe dissolution and pharmacokinetics parameters.

7
6. a)

How will you determine the shelf life of liquid dosage form?

7
b)

What are the various stability testing protocols for Parenteral dosage form? Discuss.

7
7. a)

Write a detailed note on various optimization techniques.

7
b)

Distinguish between validation and calibration. What are the government regulation regarding validation?

7
8.

Write short note on (any two):

2×7
  • a)

    Contour design

  • b)

    Manufacturing process models

  • c)

    Layout of tablet manufacturing plant

  • d)

    URS