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Download GTU B.Pharma 2018 Winter 7th Sem 2270015 Quality By Design (Qbd) And Process Analytical Technology (Pat) Question Paper

Download GTU (Gujarat Technological University Ahmedabad) B.Pharma (Bachelor of Pharmacy) 2018 Winter 7th Sem 2270015 Quality By Design (Qbd) And Process Analytical Technology (Pat) Previous Question Paper

This post was last modified on 04 March 2021

GTU B.Pharm 2018 Winter Question Papers || Gujarat Technological University


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Seat No.:

Subject Code: 2270015

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Enrolment No.

GUJARAT TECHNOLOGICAL UNIVERSITY

B.Ph. - SEMESTER- VII EXAMINATION — WINTER-2018

Subject Name: Quality by Design (QbD) and Process Analytical Technology (PAT)

Time: 10:30AM TO 01:30PM

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Instructions:

  1. Attempt any five questions.
  2. Make suitable assumptions wherever necessary.
  3. Figures to the right indicate full marks.
  1. (a) Discuss the Process performance and product quality monitoring system as an element of ICH Q10 Pharmaceutical Quality System. (06)
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  3. (b) Draw the CTD triangle and Explain the Module 5 Clinical study reports. (05)
  4. (c) Write a note on HACCP (Hazard Analysis and Critical Control Points). (05)
  5. (a) Define QbD. Discuss the elements of QbD. (06)
  6. (b) Write two primary principles of QRM and Draw the flow chart of typical Quality Risk Management Process. (05)
  7. (c) Write a note on PAT tools. (05)
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  9. (a) Explain the Ishikawa Diagram that used-as-a Risk Assessment Tool. (06)
  10. (b) Define PAT. Discuss scope and principle of PAT. (05)
  11. (c) Explain Yate’s method for optimization with example. (05)
  12. (a) Explain the terminology QTPP and CPP with suitable example with respect to QbD. (06)
  13. (b) What is Risk Priority Number? Explain with any Risk Assessment Example. (05)
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  15. (c) Write the total number of experiments and treatment combination and interaction chart for 32 Factorial design. (05)
  16. (a) Compare the Traditional and QbD approach for Pharmaceutical product supply. (06)
  17. (b) Explain with example 1) CQA 2) CMA (05)
  18. (c) Write about need of QbD for Pharma sector. (05)
  19. (a) Discuss challenges for implementation of QbD. (06)
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  21. (b) Explain the Real Time Release Study of PAT. (05)
  22. (c) Explain the mapping of CMA and CPP to CQAs with example. (05)
  23. (a) Explain the CTD module 3 Quality in detail. (06)
  24. (b) Explain the Design Space. (05)
  25. (c) Explain the control strategy approach for Quality product. (05)
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Date: 28/11/2018

Total Marks: 80

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