B.PharmSemester 82024-25Pharmaceutical Product DevelopmentBP813ET

Pharmaceutical Product Development (BP813ET) - AKTU Question Paper 2024-25

B.Pharm · Semester 8 · Free PDF Download

This is the official AKTU Pharmaceutical Product Development Previous Year Question Paper for B.Pharm Semester 8, academic session 2024-25. Published by Dr. A.P.J. Abdul Kalam Technical University (AKTU/UPTU), Lucknow. Free PDF download — no login required.

Course:B.Pharm
Semester:Semester 8
Session:2024-25
University:AKTU / UPTU

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Questions Asked in 2024-25

Pharmaceutical Product Development (BP813ET) — extracted question text · 75 marks · 3 Hours

Section AAttempt all questions in brief. 10 x 2 = 20
  • a
    Define preformulation
  • b
    How will you differentiate bet ween manufacturing and quality control testing
  • c
    Name any two solubilizers comm only used in pharmaceuticals
  • d
    State any two regulatory cons iderations for packaging materials
  • e
    Illustrate the concept of Quality by Design (QbD)
  • f
    Why is stability testing impor tant in product development?
  • g
    Differentiate between directly compressible vehicles and conventional diluents
  • h
    Evaluate the role of excipien ts in NDDS in enhancing drug delivery. i. Mention two key characteristi cs of a good semi-solid excipient j. What are non-ionic surf actants? Give one example
Section BAttempt any two parts of the following: 2 x 10 = 20
  • a
    Write a detailed note on pack aging materials used for sterile dosage forms with relevant examples
  • b
    Design a suitable formulation strategy for a poorly water-soluble drug
  • c
    Evaluate the role of cyclodext rins in enhancing solubility a nd stability of APIs with examples
Section CAttempt any five parts of the following: 7 x 5 = 35
  • a
    Classify excipients used in parenteral formulations and expl ain any one class
  • b
    Explain the application of sur factants in formulation of emulsions and suspensions
  • c
    Discuss the objectives of pha rmaceutical product development
  • d
    Analyze the significance of optimization techniques in formulation development
  • e
    List and explain key steps in manufacturing solid dosage forms
  • f
    Evaluate the need for quality control in packaging material selection
  • g
    Discuss the importance of emu lsifying agents in pharmaceutical suspensions

Question text is extracted from the official AKTU question paper PDF above. Check the original PDF for equations, diagrams and complete wording. Extracted: 2026-08-23.

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