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Roll No.
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Total No. of Pages : 01
Total No. of Questions : 06
M.Pharmacy (Pharmaceutical Quality Assurance) (2017 & Onwards)
(Sem.-2)
PHARMACEUTICAL MANUFACTURING TECHNOLOGY
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Subject Code : MQA-204T
Time: 3 Hrs.
M.Code: 76353
Max. Marks: 75
INSTRUCTIONS TO CANDIDATES :
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- Attempt any FIVE questions out of SIX questions.
- Each question carries FIFTEEN marks.
- A) Enlist the factors influencing storage of raw materials and finished products in a pharmaceutical plant. (7.5)
B) Write a note on production scheduling. (7.5) - A) Write briefly about CIP and SIP with respect to parenteral manufacturing plant. (7.5)
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B) Discuss the area planning for a sterile product manufacturing pharmaceutical plant. (7.5) - A) Write a note on spheronization and its applications. (7.5)
B) Give a schematic representation for manufacturing soft gelatin capsules. Describe the in-process quality control tests for this process. (7.5) - Write briefly about :
A) Bubble packs (5)--- Content provided by FirstRanker.com ---
B) Plastic pouches (5)
C) Glass containers and types (5) - What is meant by QbD? Mention its advantages and limitations. Discuss the process for applying QbD for designing drug products. (15)
- What is PAT? Discuss the key features of PAT and its advantages. (15)
NOTE : Disclosure of Identity by writing Mobile No. or Making of passing request on any page of Answer Sheet will lead to UMC against the Student.
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M-76353
(S31)-2756
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