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