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Industrial Pharmacy I is that subject of B Pharmacy Semester 5 which enable the scholar to grasp and appreciate the influence of pharmaceutical additives and various pharmaceutical dosage forms on the performance of the drug product.

Previous Year Question Papers of Industrial Pharmacy I

The previous year question papers is uploaded by Carewell Pharmacy which is based on AKTU [ Dr. APJ Abdul Kalam Technical University ].

There is a Table of Content given below which help you to find out your required Year Question Paper. You can click on particular year which you want to redirect.

💡 Table of Content
  1. Prev. Yr Papers of Industrial Pharmacy I [ 2020 ]
  2. Prev. Yr Papers of Industrial Pharmacy I [ 2021 ]
  3. Prev. Yr Papers of Industrial Pharmacy I [ 2022 ]


Previous Year Question Papers of Industrial Pharmacy I [ 2020 ]

SECTION A 
Ques.1 Ans. all ques. in brief [ 10*2=20 ]
  1. Name the type of drug as per BCS Classification.
  2. What are the objectives for study of physiochemical characterization of drug substance ?
  3. What is crystal bridging during wet granulation.
  4. What are various non Pharmacopoeial test conducted for evaluation of tablets ?
  5. Write in brief about IPQC test for capsule.
  6. Draw the labeled diagram of slugging machine.
  7. Amorphous or crystalline drug which will give more stable dosage form and why ?
  8. What are WFI and sterile WFI, how they are different ?
  9. What is Vapour tap and how it is significant ?
  10. Name all types of glass used in pharmaceutical packaging.

SECTION B 
Ques.2 Ans. any two ques. of the following [ 2*10=20 ]
  1. What are various defect in tablets and how they may be rectified, explain in detail ?
  2. How hard gelatin capsules shells are filled. Discuss about equipment used and principle for hard gelatin capsule filling.
  3. What are selection criteria for containers and closures for parenteral ? How you will do cleaning of containers and closure ?

SECTION C
Ques.3 Ans. any five ques. of the following [ 5*7=35 ]
  1. What are various aims and objectives for preformulation and how to proceed for preformulation ?
  2. Write note on physics of Tablet.
  3. How to evaluate suspension ?
  4. Write various advantages and disadvantages for parenteral products.
  5. How particle size of drug may affect development of stable dosage form ?
  6. How will you formulate tooth paste, explain and give preparation method for the same.
  7. What are various parts of aerosol valve ? Explain with diagram.

Previous Year Question Papers of Industrial Pharmacy I [ 2021 ]

SECTION A 
Ques.1 Ans. all ques. in brief [ 10*2=20 ]
  1. What do you mean by preformulation studies ?
  2. How are drugs classified as per BCS ?
  3. What is the role of binders in manufacturing tablets ?
  4. Define super-disintegrates with examples.
  5. What are the various size of capsules available for human use ?
  6. What do you mean by Bloom Strength ?
  7. Explain significance of isotonicity in parenteral formulation.
  8. What is the function of propellants in aerosol system ?
  9. Define aseptic processing.
  10. Define tamper evident packaging.

SECTION B 
Ques.2 Ans. any two ques. of the following [ 2*10=20 ]
  1. Discuss in detail about various test which are generally done to maintain the quality control of tablets.
  2. What are the advantages of capsules as dosage form ? Discuss in details about various mechanism of filling powder in hard gelatin capsules.
  3. Classify different types of parenteral products. How are parenteral products evaluated for quality control ?

SECTION C
Ques.3 Ans. any five ques. of the following [ 5*7=35 ]
  1. What is the significance of pKa in preformulation studies ?
  2. Discuss the principle and working of Rotary tablets press in details.
  3. How is coating of tablets beneficial ? Discuss working of a coating pan.
  4. Elaborate the process of manufacturing of hard gelatin capsule shell.
  5. How are dry powders for injection prepared by Lyophilization ?
  6. What are the various components of Aerosol product ? Explain significance of each.
  7. Discuss various quality control tests of glass as a packaging material.


Previous Year Question Papers of Industrial Pharmacy I [ 2022 ]

SECTION A 
Ques.1 Ans. all ques. in brief [ 10*2=20 ]
  1. List various components of pharmaceutical aerosol.
  2. Differentiate between dextrorotatory and levorotatory.
  3. What are the basic steps of process of dry granulation ?
  4. What are the glidant ?
  5. What is deflocculated system ?
  6. What are the different sources of pyrogenic contamination ?
  7. What are the factor affecting the drug absorption from ophthalmic route ? 
  8. Enlist the optimizable properties of powder layering technique ? 
  9. Why gelatin is the most preferred shell formulating material for capsules ?
  10. Which type of glass consume the least volume of acid in Powdered Glass Test ?

SECTION B 
Ques.2 Ans. any two ques. of the following [ 2*10=20 ]
  1. Describe various materials used for packaging of pharmaceutical products with regards to their benefits, limitations and remedy to overcome such limitations.
  2. Illustrate the rotary die process with the help of flow chart, diagram and underlying principle.
  3. Explain the in-process and finished product quality control tests for tablet dosage form based on pharmacopoeia standards and specifications.

SECTION C
Ques.3 Ans. any five ques. of the following [ 5*7=35 ]
  1. Explain various processing problems of uncoated tablet and their remedies.
  2. Discuss the evaluation of ophthalmic preparation as per pharmacopoeia standards and specifications.
  3. Illustrate the process to prepare lyophilized parenteral products with the help of well labelled diagram.
  4. Explain equipment for manufacture of pellets with well labelled diagram.
  5. Discuss the application of pre-formulation considerations in the development of tablet dosage form with appropriate industry related case study.
  6. Discuss briefly about formulation of cold cream.
  7. Discuss the in-process and finished product quality control tests for pharmaceutical aerosols based on pharmacopoeia standards and specifications.