Industrial Pharmacy M.Pharm Question Bank : web.tnmgrmu.ac.in

Name of the University : The Tamilnadu Dr. M.G.R. Medical University
Degree : M.Pharm DEGREE EXAMINATION
Subject Code/Name : 2902/Industrial Pharmacy
Year : I
Paper : II
Document Type : Question Bank
Website : web.tnmgrmu.ac.in

Download Model/Sample Question Paper :
2011-2014 : https://www.pdfquestion.in/uploads/web.tnmgrmu.ac.in/PHYSIOTHERAPY/3850-262902KY.pdf

TN MGRMU Industrial Pharmacy Question Paper

MAY 2011 :
[KY 341] Sub. Code: 2902
M.PHARM. DEGREE EXAMINATION

Related : TNMGRMU Modern Pharmaceutical Analytical Techniques M.Pharm Question Bank : www.pdfquestion.in/3848.html

(Regulations 2010)
Candidates admitted from 2010-2011 onwards
Branch I : PHARMACEUTICS
Paper II : INDUSTRIAL PHARMACY
Q.P. Code : 262902
Time : Three hours
Maximum : 100 marks
Answer All questions :
I. Essay Questions : (6 x 10 = 60)
1. Discuss in detail the formulation and evaluation of Parenteral products.
2. Discuss about Production management in Pharma Industries.
3. Describe Plastic containers used in packing of Pharmaceutical preparations. Add a note on evaluation of plastic containers.
4. Explain GMP guidelines for Sterile preparations.
5. Discuss about the Heat sterilization methods.
6. Explain in detail the filling of Hard gelatin capsules. Add a note on evaluation of capsules.
II. Write Short Notes : ( 8 x 5 = 40 )
1. Objectives and Defects in Tablet coating.
2. Multivitamin Products.
3. How can shelf life be determined by accelerated stability method?
4. Optimization parameters.
5. Multiple Emulsions.
6. Industrial hazards and preventive measures due to fire accident.
7. Formulation of Dry syrup with example.
8. TRIPS and WTO.

October 2011

Answer ALL questions in the same order. :
I. Elaborate on :
1. What is Optimization? Discuss the various optimization techniques in formulation and processing.
2. Explain in detail about the significance of Pilot plant scale up study and large scale manufacturing techniques of Injections and Liquid orals.
II. Write notes on :
1. Production Management.
2. Physics of tablet compression.
3. Techniques for the study of crystal properties and polymorphism.
4. Pharmaceutical aspects related to GATT and TRIPS.
5. Physicochemical and biological factors affecting stability of drugs.
6. Determination of shelf life by Accelerated Stability Testing.
7. Evaluation of plastic containers used in packaging of pharmaceutical preparation.
8. Industrial hazards and preventive measures due to fire accident.
9. Quality Assurance.
10. Multivitamin Products.

May 2012

Answer ALL questions in the same order. :
I. Elaborate on:
1. Discuss in detail about GMP consideration and material management for the Pharmaceutical Industry.
2. Differentiate Consolidation and Compression with definitions. Write a detailed note on the distribution and measurement of forces and physics of Tablets.
II. Write notes on:
1.Thermosettings.
2. World Trade Organization.
3. Describe briefly on search methods used in optimization.
4. Techniques used to find out the crystal properties.
5. Define Sterilization and briefly explain types of sterilization.
6. Formulation of dry syrup with example.
7. Describe about the preventive measures due to electrical hazards.
8. ISO 9000 series.
9. Blood Products.
10.Pilot plant scale up preparation for liquid orals.

October 2012

I. Elaborate on : Pages Time Marks
1. Explain the role of various Physico-Chemical characteristics of a new drug molecule in preformulation studies.
2. Discuss in detail about different types of Pharmaceutical containers and closures including their merits and demerits.

II. Write notes on :
1. Material management in Pharma Industry.
2. Effect of particle size, moisture content and lubrication on strength of Tablets.
3. Intellectual Property Rights.
4. Significance of Pilot plant scale up study.
5. ISO 9000 series.
6. Optimization methods.
7. Multiple Emulsion.
8. Sterilization of various Injectables.
9. Overages and ICH guidelines.
10. Hazards and safety measures due to mechanical and electrical equipments used in Pharma Industry.

April 2013

I. Elaborate on :
1. Define Pharmaceutical Packing? What are the salientfeatures of packing material? Discuss about the packing of glass container and Plastic containers.
2. Define stability. What are the different types of stability and explain briefly about any two methods.

II. Write notes on :
1. Preformulation study on polymorphism.
2. Differentiate moist heat and dry heat sterilization.
3. Patent Laws.
4. Prediction of shelf life by accelerated stability method.
5. Chemical Hazards and their preventive measures.
6. Physics of Tablets.
7.Process Validation.
8. Define Optimization and explain about Lagrangian method.
9. Describe about the production planning and sales forecasting.
10. Multivitamin Products.

October 2013

I. Elaborate on : (2 x 20 = 40)
1. a) Explain production planning and control in Pharmaceutical Industry.
b) Explain in detail about physicochemical factors affecting stability of drugs.
2. Discuss in detail about different types of Pharmaceutical containers and closures including their merits and demerits.

II. Write notes on :
1. Material management in Pharma Industry.
2. Effect of particle size, moisture content and lubrication on strength of Tablets.
3. Intellectual Property Rights
4. Significance of Pilot plant scale up study.
5. ISO 9000 series.
6. Optimization methods.
7. Multiple Emulsions.
8. Sterilization of various Injectables.
9. Overages and ICH guidelines.
10. Hazards and safety measures due to mechanical and electrical equipments used in Pharma Industry.