Professional Documents
Culture Documents
FOR
POSTGRADUATE PROGRAMME
IN
MASTERS OF PHARMACEUTICAL
(BIOTECHNOLOGY) 2011
It is with great pleasure and honour that I write a forward for the Model scheme of
instruction and syllabi for the Undergraduate Pharmaceutical Education Programme prepared by
the All India Board of Pharmaceutical Education with Dr. S.Y. Ghabe as its Chairman and other
members. All India Council for Technical Education has the onerous responsibility for uniform
development and qualitative growth of the Technical Education system and preparation of syllabi
to maintain uniform standards throughout the county. In pursuance to clause 10 (2) of the AICTE
Act 1987 AICTE has the objective of bringing about uniformity in the curriculum of Pharmaceutical
Education. In that direction, the efforts of the All India Board of Pharmaceutical Education has been
quite commendable and praiseworthy. A painstaking effort was made by the Chairman, members
of the Board and various working groups composed of experts from leading institutions in framing
of the Instruction and Syllabi. The Board was ably assisted by the official of the Academics Bureau
in successfully organizing the meetings making available necessary documents and follow up action
on the minutes of the meetings.
Chairman
Total 60
Text Books:
Reference books :
Robert M. Silverstein, Francis X. Webster, David J. Kiemle, 2009. “Spectrometric identification of
organic compounds”. 7th Ed. John Wiley & Sons
Pavia D. L., 2009. “Introduction to spectroscopy”. 4th, Belmont CA
Munson & Munson, “Pharmaceutical analysis: modern methods”. edited by James W. Munson, New
York : M. Dekker
Kenneth A. Connors, 2007. “A Textbook Of Pharmaceutical Analysis” 3rd Ed. Wiley India-wse
Jens Thuro Carstensen, 2001. “Advanced pharmaceutical solids” Marcel Dekker, New York
Joseph B. Lambert, Scott Gronert, Herbert F. Shurvell, David Lightner, Robert Graham Cooks, 2010.
“Organic structural spectroscopy”, 2nd Ed. Pearson Education, Limited.
It is strongly recommended that some standard book/s be used for practicals. The choice of
book/s is left to the concerned teachers.
Suggested List of Laboratory Experiments :
S.No
1 Estimation of two drugs by simultaneous equation method and absorbance ratio method.
2 Calibration of UV spectrometer for wavelength and stray light.
3 Analysis of drugs by second derivative UV spectrometry.
4 Determination of pK value by UV visible spectrometry.
5 Calculation of λmax values using Woodward Fisher rules.
6 Study of hydrogen bonding using IR spectrometer.
7 Interpretation of IR spectra.
8 Calibration of IR spectrometer using standard polystyrene film.
9 Interpretation of 1D proton NMR spectrum of simple compounds (10-12 carbons).
10 Interpretation of 1D 13C NMR spectrum of simple compounds (10-12 carbons).
11 Calculation of carbon chemical shifts for various carbons such as sp3, sp2, sp carbon etc.
12 Assignment of m/z values to various fragments in the mass spectrum.
13 Qualitative and quantitative analysis using HPTLC.
14 Analytical method development for three component mixture using HPTLC.
15 Calibration of HPLC instrument for flow rate & wavelength.
16 Determination of theoretical plate, HETP, resolution, tailing factor for two component
..mixture
17 Determination of caffeine content in tea/ coffee/ other beverages.
18 Quantitation using different methods such as area normalization, one point, two point
method with the help of internal standard.
19 Determination of melting point & heat of fusion using DSC.
20 Determination of glass transition temperature using DSC.
21 Interpretation of ORD and CD spectrum.
Suggested List of Assignments/Tutorial : N A
Name of the Course :Computer and Statistics
Course code: S1-MPB-3 [ T ] Semester : I
Duration : 60 Hrs[ T ], 60 Hrs [ P ] Maximum Marks : 100
Teaching Scheme Examination Scheme
Theory : 04 Hrs/week Mid Semester Exam: 20 Marks
Tutorial: Hrs/week [ If required ] Assignment &Quiz: 10 Marks
Practical : 04 Hrs/week End Semester Exam: 70 Marks
Credits : 04 Each [ T & P ]
Aim :-
Objective :-
S. No
1 To train students in basics of computer hardware.
2 To train them on hands on experience in use of different software.
3 To teach them applications of computers in different areas of Pharmacy.
4 To train the students for applications of various statistical methods available for
analysis of data.
Pre-Requisite:-
S. No
1 A 10 + 2 level mathematics & rudimentary knowledge of computers.
2 A B, Pharm. Degree from any institution approved by AICTE or its equivalent.
Contents Hrs
Computers
Unit -1 Hardware: Current hardware & their performance, New devices / technology 03
useful in teaching & research like Cameras, Scanner, touch screens, tablets,
projection devices etc. Basic idea of computer networking.
Unit -2 Operating systems: Common operating systems used in day to day task & 15
instrumentation like Windows, Linux & Unix (only interface and basic
commands).
Unit -3 Language: Evolution of computer languages. Common languages used in 06
scientific fraternity (no specific language detailing is required).
Unit -4 Software: 05
Idea of popular soft ware’s like MS Office, structure drawing software’s,
chemical structure visualizing software’s, statistical software’s & mathematical
software, reference managing software’s (only introduction).
Unit -5 Web page design: Need, concept and use of HTML. 08
Unit -6 Databases: Meaning, Need and creating table, record creating and maintenance. 05
Unit -7 Internet concept: History, creating internet connection, common problems & 06
solutions.
Unit -8 Important Databases of free domain: 05
Patents, Pub med, Pubchem, Science direct, protein database.
Statistics
Unit -1 Data & Graphs. 03
Unit -3 Sampling. 04
Unit -5 Optimization. 06
Pre-Requisite:-
S. No.
1 Basic knowledge in microbiology, enzyme kinetics, fermentation & basic extraction &
other related processes.
2 A B. Pharm. degree from any institution approved by AICTE or its equivalent.
Contents Hrs
Unit -1 Historical development of bioprocess technology, An overview of traditional and 03
modern applications of biotechnological processes, general requirements of
fermentation processes.
Unit -2 Isolation, Screening and Application of Industrially Important Microbes: Primary 04
and secondary screening, maintenance of stock cultures, strain improvement for
increased yield.
Unit -3 Design of Fermentation Process: 04
a. Detailed study of the design and operation of bioreactor, ancillary parts and
functions: impeller design & agitation power requirements: on-line
measurement and control of dissolved oxygen, carbon dioxide,
temperature, pH and foam.
b. Types of reactors – CSTR, tower, air-lift, bubble-column, packed bed,
hollow fiber –configuration and applications.
Unit -4 Mass Transfer – theory, diffusional resistance to oxygen transfer, Oxygen 08
requirements of micro organism, measurement of mass transfer coefficient and
factors affecting them: effects of aeration and agitation on mass transfer, supply
of air, air compressing, cleaning and sterilization of air, air sampling and testing
standards for air purity
Unit -5 Rheology: Rheological properties of fermentation systems and their importance 04
in bioprocessing.
Unit -6 Fermentation Kinetics: Reaction kinetics: Michaelis Menten constant and Monod 06
equation derivations for biomass estimation: Lineweaver–Burke plot.
Unit -7 Cultivation Systems: closed, semi-open and open systems: graphical plots 06
representing the above systems: use of immobilized culture systems to prepare
fine chemicals.
Unit -8 Scale up of Fermentation Process: Principles, theoretical considerations and 04
techniques used
Unit-9 Downstream Processing: Theory, equipment design and operation, methods, 08
filtration, solvent extraction, chromatographic separation, crystallization,
turbidity analysis and cell yield determination metabolic response assay,
enzymatic assay, bioautography, techniques for disruption of cells for product
recovery.
Unit-10 Bioprocess of the following Industrially Important Microbial Metabolites: 09
Alcohol, Citric acid and Lactic acid, Penicillin, Streptomycin, Griseofulvin,
Cephalosporins, Amphotericin B, Rifampicin, Vitamin B12 and Riboflavin,
Glutamic acid and Lysine, Nucleotides : Cyclic AMP & GMP.
Unit-11 Computer control of fermentation processes & Regulatory aspects: System 04
configuration and applications, Regulations governing the manufacture of
biological products.
Total 60
Text Books: N A
Reference books :
1. L.E. Casida, “Industrial Microbiology” John Wiley and Sons Inc.
2. B.M. Miller and W. Litsky, “Industrial Microbiology”. McGraw Hill.
3. H. Peppler, “Microbial Technology”. Vol. I & II. Academic Press, New York.
4. Vedpal S Malik and Padma Sridhar, “Industrial Biotechnology”.
5. C Rainbow and AH Rose, “Biochemistry of Industrial Microorganisms”.
6. F.M Asubel, “Current protocols in molecular biology”. Vol. I & II, John Wiley Publishers.
7. Gianeario Lancini and Rolando Lorenzetti, 1992. “Biotechnology of antibiotics and other bioactive
microbial metabolites”. Science Pub Inc.
8. I J Dunn, E. Heinzle, J Ingham, J. E. Prenosil, “Biological reaction engineering”
9. Bioreactor design and product yield: Butterworth and Heinemann.
10. Enzyme assays – a practical approach: Robert Eisenthal and Michael J Danson.
11. Fermentation and biochemical engineering handbook: Henry C Vogel
12. F. C. Webb, “Biochemical Engineering”. McGraw Hill, New York.
13. R. Steel, “Biochemical Engineering”. Chemical Publishing Co. Inc. New York.
14. Bailey and Ollis, “Biochemical Engineering Fundamentals”. McGraw Hill, New York.
15. Aiba S., Humphrey. A. E and Milli N. F , “Biochemical Engineering”. Academic Press, NY.
16. Paulin M. Doran, “Bioprocess Engineering Principles”. Academic Press, London.
17. It is strongly recommended that some standard book/s be used for practicals. The choice of
book/s is left to the concerned teachers.
Suggested List of Laboratory Experiments :
1. Isolation and secondary screening of industrially important microorganisms.
2. Strain improvement (for increased yield) by stress inducers.
3. Preparation, calibration, and standardization of a bioreactor.
4. Power calculations, KLa determinations and MTR calculations of a typical bioprocess.
5. Construction of growth curve and determination of specific growth rate and doubling time.
6. Biomass estimation by monitoring protein synthesis and sugar depletion.
7. Enzyme kinetic study
a. Effect of metal ion concentration.
b. Effect of pH.
c. Effect of temperature.
d. Effect of varying substrate concentration.
e. Kinetic parameter calculations.
8. Protein separation by aqueous two-phase partitioning.
9. Fermentation process of alcohol and wine production.
10. Fermentation of vitamins and antibiotics.
11. Whole cell immobilization engineering
a. Using various polymers.
b. Study of physical characteristics.
c. Comparison of efficacy of immobilized and free cells.
12. Downstream processing,
a. methods of cell disruption.
b. typical isolation process for antibiotics.
c. purification by chromatographic techniques.
13. Microbiological assay of antibiotics.
14. Thermal death kinetics of bacteria and its applications.
Suggested List of Assignments/Tutorial : N A
Text Books: N A
Reference books: Choice is left to the institution faculty.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Drug Regulatory Aspect and IPR
Course code: S3-MPB-1 [T ] Semester : III
Duration : 60 Hrs Maximum Marks : 100
Teaching Scheme Examination Scheme
Theory : 04 Hrs/week Mid Semester Exam: 20 Marks
Tutorial: Hrs/week [ If required ] Assignment & Quiz: 10 Marks
Practical : Hrs/week [ N A ] End Semester Exam: 70 Marks
Credits : 04
Aim :-
Objective :-
S. No
1 To impart information on various drug regulatory aspects involved in the profession.
2 To teach the import / export related regulations with respect to some countries.
3 To make the students understand the importance & implications of IPR & related
matters.
4 To train the students in GMP & the latest developments there.
Pre-Requisite:-
S. No
1 A course at UG level regarding regulatory aspects, law governing Pharmacy profession.
2 A B. Pharm. Degree from any institution approved by AICTE or its equivalent.
Contents Hrs
Unit-1 DRUG REGULATORY ASPESTS 40
a) Drug Regulatory Aspects (India) – 10
1. Indian drug regulatory authorities, Central and State regulatory bodies
(FDA).
2. Drugs and Cosmetics Act and Rules with latest Amendments (selective).
3. Special emphasis – Schedule M and Y.
4. New Drugs – Importation, Registration, development, clinical trials, BE
NOC & B.E. studies.
5. Various licenses – Test lic., Import lic. for testing of drugs and API’s, Mfg.,
Contract and Loan license manufacturing.
b) Good Manufacturing Practices (GMP) – 12
1. Indian GMP certification, WHO GMP certification.
2. ICH guidelines for stability testing and other relevant ones (Q1 – Q10).
3. Export permissions and manufacturing for semi-regulated countries.
4. Understanding of the plant lay-outs with special emphasis on the
environment & safety. (HVAC, water systems, stores management,
effluent etc.).
5. Quality Assurance and Quality Control – Basic understanding for in-built
quality.
c) Drug Regulatory Aspects (International & highly regulated markets) – 18
1. US Requirements – (for Generic Drugs especially formulations).
2. CDER, INDA, NDA, ANDA’s (types), CTD Formats of dossiers, E-
submission, US DMF (various types), IIG Limits, 0rphan Drugs, vanilla
ANDA’s, exhibit/pivotal batches, validation batches, various guidance
issued by CDER, OGD, Orange Book (and patents), RLD (reference listed
drug) for BE studies and the norms for US submission, bioequivalence
and dissolution recommendations, packaging, stability studies and the
product information leaflet, US FDA inspection (audits), pre-approval
inspections and approvals.
3. European Union Requirements –
4. All the aspects for European registration of formulations for generic
drugs sale in the European markets under EU. EMEA guidelines on
various aspects as above (C 1).
5. A brief introduction to the guidelines for Japan, Australia, South Africa,
Rest of the World (ROW) and South & Latin American countries.
6. GMP audits, role of quality assurance, product approvals and supplies.
Unit-2 INTELLECTUAL PROPERTY RIGHTS (IPR) 20
a) Introduction to IPR & Patents – Development of IP law in India, IPR regime,
introduction to IP laws in India, role of IP in pharma industry growth.
b) Patenting in India – Introduction, patent legislation, Indian Patents Act 1970
and amendments, procedure for patent application, grant and opposition
proceedings, patent licensing, patent infringement proceedings, IPAB – role and
functions (IP Appellate Board), Indian IP case laws.
c) American & European patent system – Requirements for patenting, utility,
novelty non-obviousness, patent specification & claims, patent infringement and
doctrine of equivalents, federal circuit and patent system in Europe.
d) International treaties and conventions on IPR - Paris convention, PCT – an
introduction, PCT application & general rules, WTO / GATT system & Uruguay
TRIPS, WIPO.
e) Hatch Waxman Act and amendments, FDA Medicare Modernization Act,
2003.
f) Introduction to geographical indication / trademark/ copyright: filing
procedures.
g) Patent search, patent analysis & patent drafting.
h) Allied Patents Related Issues: Exploitation of patent, abuse of patents,
compulsory licensing, infringement analysis, drug-patent linkage.
Total 90
Text Books:
It is strongly recommended that some standard book/s be used for practicals. The choice of book/s is
left to the concerned teachers
Reference books :
1. CDSO publications and updates of drug and Cosmetics act and rules (Govt. of India).
2. CDER Publications and Guidance
3. EMEA Publications and Guidance
4. Orange Book, ICH guidelines, Indian Patents Act
5. Country specific Regulatory Guidelines (available from internet)
6. Govt. Publications on issues affecting sales, distribution, manufacturing, excise, etc.
7. J. D. Nally, “Good manufacturing Practice for Pharmaceuticals” Informa Healthcare.
8. I. Kanfer & L. Shargel, “Generic Product Development BE issued” Informa Healthcare.
9. R. A. Guarino, “New Drug Approval Process. The Global challenges”. Informa Healthcare.
10. Watcher and Nash, “Pharmaceutical Process Validation”. Marcel Dekker.
11. Pharmaceutical Product Dev. IVIVC by Murthy, Sunkara and David
12. USPTO and WIPO Guidelines, Indian Patents Act
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Research Work Seminar
Course code: S3-MPB-2 [ P ] Semester : III
Duration : 120 Hrs Maximum Marks : 100
Teaching Scheme Examination Scheme
Theory : Hrs/week [ N A ] Mid Semester Exam: 30 Marks
Tutorial: Hrs/week [ N A ] Assignment & Quiz: Marks [ N A ]
Practical : 08 Hrs/week End Semester Exam: 70Marks
Credits : 04
Aim :-
Objective :-
S. No
1 To effectively present the research work carried out by the student.
Pre-Requisite:-
S. No
1 A B. Pharm. Degree from any institution approved by AICTE or its equivalent.
Contents Hrs
S. No Nil
Text Books: N A
Reference books: The choice of literature depends on the topic selected & is left to the concerned
faculty.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Research Project
Course code: S3-MPB-3 [ P ] Semester : III
Duration : 240 Hrs Maximum Marks : 150
Teaching Scheme Examination Scheme
Theory : Hrs/week Mid Semester Exam: Marks [ N A ]
Tutorial: Hrs/week Assignment & Quiz: Marks [ N A ]
Practical : 16 Hrs/week End Semester Exam: 150 Marks
Credits : 06
Aim :-
Objective :-
S. No
1 To effectively present the research work carried out by the student.
Pre-Requisite:-
S. No
1 A B. Pharm. Degree from any institution approved by AICTE or its equivalent.
Contents Hrs
S. No NIL
Text Books: N A
Reference books: The choice of books & other literature material depends on the topic selected
& is left with the concerned faculty member.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Industrial Biotechnology
Course code: S3-MPB-4 [ T ] Semester : III
Duration : 60 Hrs Maximum Marks : 100
Teaching Scheme Examination Scheme
Theory : 04 Hrs/week Mid Semester Exam: 20 Marks
Tutorial: Hrs/week [ If required ] Assignment & Quiz: 10 Marks
Practical : Hrs/week [ N A ] End Semester Exam: 70 Marks
Credits:- 04
Aim :-
Objective :-
S. No.
1 To impart advanced level knowledge in the area of enzyme technology, fernenters &
bioreactors, & related fields.
2 To build upon the ideas about cell culture, stem cells, cloning & other important
developments in this field specially with use in Pharmacy.
3 To review recent developments in the field with reference to Pharmacy.
Pre-Requisite:-
S. No.
1 Basic knowledge in biotechnology.
2 A B. Pharm. degree from any institution approved by AICTE or its equivalent.
Contents Hrs
Unit-1 Enzyme Technology Process 5
Chemically and genetically modified enzyme. Isolation, purification and
modification in enzymes. Enzymes as therapeutics, enzymes in drug delivery
design. Industrial enzymes in drug development: Penicillin amidase,
carbohydrase enzymes, chymosin from calf stomach.
Unit-2 Immobilization 4
Introduction, methods of immobilization, selection of methods, entrapment and
encapsulation, characterization, kinetics of immobilized biocatalysts,
immobilized cells and application. Potentials of immobilized bioactives.
Unit-3 Design & Construction of Fermenters & Bioreactors 8
Detailed study of the design and operation of different types of fermenters,
ancillary fittings, transfer of spore suspension, transfer of inoculums from seed
tank to fermenter, impeller design and agitator power requirements,
measurement and control of dissolved oxygen, carbon dioxide, temperature, pH
and foam. Aeration, agitation and mass transfer in fermentation, Supply of air
cleaning and sterilization of air, methods of providing air, air compression and
air sterilization methods. Types of bioreactors, modeling of immobilized
biocatalyst reactors, bioreactors applications.
Unit-4 Fermentation Technology 6
Media, solid state and liquid phase fermentation, surface culture, submerged and
batch culture, continuous fermentation. Strain improvement. Industrial
fermentation of alcohol, citric acid, antibiotics, enzymes, vitamins, dextran,
starch, alcohol and prostaglandins. Yeast and its production. Production of single
cell proteins
Unit-5 Principles of Cell Culture & Preparation Techniques 8
Preparation of tissue culture media, sterilization of plant materials, plant cell
culture, isolation of single cells from intact plant. Growth determination and
medium analysis. Hormonal control of growth. Initiation and maintenance of
callus cultures.
Unit-6 Applications of Cell Culture Techniques 6
Cell isolation, in vitro cellular uptake studies, cell biochemistry study, secondary
metabolite production, fermentation & genetic manipulation. Embryogenesis,
embryo cloning, cell cloning prospects and perspectives. Therapeutic novel
molecular expression, Trait improvement.
Unit-7 Plant & Animal Cell Culture 7
Types of cultures: Callus culture, Meristem-tip culture, organ culture (Flower and
fruit organ culture), microspore and anther culture, protoplast culture, primary
culture, continuous culture, cell fusion micropropagation, Modification through
transformative cell culture, Ti-plasmids. Regeneration of plants. Production of
secondary metabolites. Protoplast microinjection. Mutagenesis technique in
plant tissue culture. Pest resistance, herbicide tolerance, peptidal hormones,
production and applications.
Unit-8 Cell Replacement, Stem Cells, Cloning & Regenerative Medicine 6
Nuclear transplantation and cell replacement therapy, germ line stem cells,
therapeutic applications, tissue-engineering and regenerative medicine.
Unit-9 Immunological Techniques As Advanced Biotechnological Tools 10
Antigen-antibody reactions, basics of immunodiagnostics, immunoprecipitation-
agglutination and complement fixation, isotopic and non-isotopic immunoassays.
Assessment of cell mediated immunity- Purification and bioassay of IL-I and IL-2,
cytotoxicity assays, etc. Microscopic techniques for sub cellular location of
antigen and diagnosis. Electron microscopy, avidin-biotin systems, gold labeling.
Immunofluorescence, cell separation techniques, immunosensors and Nucleic
acid based diagnostics.protein separation technique, radioimmunoassay, enzyme
immunoassay, flow injection immunoassay, Immobilization test, DNA
fingerprinting, Biosensors, Flowcytometry: Principle & Instrumentation:
Applications of Flowcytometry: Applications of immunoflowcytometry in cell
death processes, recombinant DNA vaccines.
Total 60
Text Books:
It is strongly recommended that some standard book/s be used for practicals. The choice of book/s is
left to the concerned teachers.
Reference books :
1. L.E. Casida, 1968. “Industrial Microbiology”, Wiley.
2. B.M. Miller and W. Litsky, “Industrial Biotechnology”.
3. H. Peppler, 1979. “Microbial Technology: Fermentation technology”, Academic Press
4. V.S. Malik and P. Sridhar, 1992, “Industrial biotechnology”, Oxford & IBH Pub. Co.
5. Vyas and Kumar, “Advances in Pharmaceutical Biotechnology”, CBS Publishers.
6. C. Rainbow and A.H. Rose, 1969. “Biochemistry of Industrial Microorganisms”, Academic Press.
7. I. Freshney, 1986. “Animal cell culture: a practical approach”, IRL Press.
8. S.R. Maloy, J.E. Cronan, D. Freifelder, “Microbial Genetics” Jones and Bartlett Publishers, London.
9. J.E. Bailey, D.F. Ollis, “Biochemical engineering fundamentals”, McGraw-Hill, 1986.
10. G. Lancini and R. Lorenzetti, “Biotechnology of Antibiotics and Other Bioactive Microbial
Metabolites”, Plenum Press.
11. Bioreactor Design and Product Yield, 1992. Butterworth and Heinemann.
12. R. Eisenthal and M.J. Danson, 2002. “Enzyme Assays - A Practical Approach”, Oxford University
Press.
13. H.C. Vogel, C.L. Todaro, 1997. “Fermentation and Biochemical Engineering Handbook”, Noyes
Publications.
14. It is strongly recommended that some standard book/s be used for practicals. The choice of
book/s is left to the concerned teachers.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Elective-I
Course code: S3-MPB-5 [ T ] Semester : III
Duration : 60 Hrs Maximum Marks : 100
Teaching Scheme Examination Scheme
Theory : 04 Hrs/week Mid Semester Exam: 20 Marks
Tutorial: Hrs/week [ N A ] Assignment & Quiz: 10 Marks
Practical : Hrs/week [ N A ] End Semester Exam: 70 Marks
Credits : 04
Aim :-
Objective :-
S. No
1 To enrich the knowledge of a student desirous of studying special topic / s of interest.
Pre-Requisite:-
S. No.
1 A B. Pharm. Degree from any institution approved by AICTE or its equivalent.
Contents Hrs
S. No Institution should decide the topics. 60
Text Books: N A
Reference books: The books to be referred to shall be decided by the topic / s selected.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A
Name of the Course : Research Project and Colloquium
Course code: S4-MPB-1 [ P ] Semester : IV
Duration : 540 Hrs Maximum Marks : 400
Teaching Scheme Examination Scheme
Theory : Hrs/week [N A ] Mid Semester Exam: Marks [ N A ]
Tutorial: hrs/week [ N A ] Assignment & Quiz: Marks [ N A ]
Practical : 36 Hrs/week End Semester Exam: 400 Marks
Credits : 16
Aim :-
Objective :-
S. No
1 To complete the given research project.
2 To effectively defend the work before a group of qualified evaluators.
Pre-Requisite:-
S. No
1 A B. Pharm. degree from any institution approved by AICTE or its equivalent.
Contents Hrs
S. No Nil
Text Books: N A
Reference books: Reference material to be referred to shall depend on the research project.
Suggested List of Laboratory Experiments : N A
Suggested List of Assignments/Tutorial : N A