Exam Details
| Subject | experimental design and patents | |
| Paper | ||
| Exam / Course | m.pharm | |
| Department | ||
| Organization | Gujarat Technological University | |
| Position | ||
| Exam Date | November, 2018 | |
| City, State | gujarat, ahmedabad |
Question Paper
Seat No.: Enrolment
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: 930001 Date: 15/11/2018
Subject Name: Experimental Design And Patents
Time: 10:30 AM TO 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make Suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
What is Design of Experiment? Discuss fractional factorial designs with its advantages limitations.
8
What is interaction between input factors? Describe Placket-Burman design for screening with its limitations.
8
Q.2
What is central composite design? Discuss Box-Wilson design for optimization.
8
Following table represents the results of 23 full factorial study performed to improve the yield of a process. Using Yate's method, construct the polynomial equation and comment on the equation.
Treatment
combination
a
b
ab
c
ac
bc
abc
Yield
93
76
84
80
78
85
91
75
8
Q.3
What are contour diagrams? Describe its significance with suitable examples.
8
What is model? Describe development of full and reduced model in context to experimental design.
8
Q.4
Explain following terminologies with reference to experimental design:
Experimental error ii) Input Factors iii) Responses iv) Confounding
8
Write a note on copy write and trademark protection.
8
Q.5
What is patent? Why is it needed? What are the advantages of taking patents?
8
Describe about product patent and process patent giving suitable examples.
8
Q. 6
What is patent search? Discuss the salient features of 2005 Patent Amendments in Indian Patent Act.
8
What is an invention? Describe the characteristics of patentable inventions.
8
Q.7
Explain laboratory notebook with its significance? Describe guidelines for preparation of laboratory notebook.
8
What is patent infringement? Discuss the different types of patent infringement.
8
GUJARAT TECHNOLOGICAL UNIVERSITY
M.PHARM SEMESTER EXAMINATION -WINTER 2018
Subject Code: 930001 Date: 15/11/2018
Subject Name: Experimental Design And Patents
Time: 10:30 AM TO 01:30 PM Total Marks: 80
Instructions:
1. Attempt any five questions.
2. Make Suitable assumptions wherever necessary.
3. Figures to the right indicate full marks.
Q.1
What is Design of Experiment? Discuss fractional factorial designs with its advantages limitations.
8
What is interaction between input factors? Describe Placket-Burman design for screening with its limitations.
8
Q.2
What is central composite design? Discuss Box-Wilson design for optimization.
8
Following table represents the results of 23 full factorial study performed to improve the yield of a process. Using Yate's method, construct the polynomial equation and comment on the equation.
Treatment
combination
a
b
ab
c
ac
bc
abc
Yield
93
76
84
80
78
85
91
75
8
Q.3
What are contour diagrams? Describe its significance with suitable examples.
8
What is model? Describe development of full and reduced model in context to experimental design.
8
Q.4
Explain following terminologies with reference to experimental design:
Experimental error ii) Input Factors iii) Responses iv) Confounding
8
Write a note on copy write and trademark protection.
8
Q.5
What is patent? Why is it needed? What are the advantages of taking patents?
8
Describe about product patent and process patent giving suitable examples.
8
Q. 6
What is patent search? Discuss the salient features of 2005 Patent Amendments in Indian Patent Act.
8
What is an invention? Describe the characteristics of patentable inventions.
8
Q.7
Explain laboratory notebook with its significance? Describe guidelines for preparation of laboratory notebook.
8
What is patent infringement? Discuss the different types of patent infringement.
8
Other Question Papers
Subjects
- advanced medicinal chemistry
- advanced organic chemistry-i
- advanced organic chemistry-ii
- advanced pharmacology ii
- advanced pharmacology-i
- advances in drug delivery system
- advances in pharmacology
- applied pharmacotherapeutics - ii
- applied pharmacotherapeutics-i
- audits and regulatory compliance
- biological evaluations & clinical research
- cellular and molecular pharmacology
- clinical and hospital pharmacy
- clinical pharmacy practice
- clinical research and pharmacy practice
- clinical research and regulatory affairs
- clinical research regulations
- cosmetic and cosmeceuticals
- documentation and regulatory writing
- drug design and discovery
- drug regulation and regulatory authority
- experimental design and patents
- global regulatory requirements
- gmp, glp and validation
- good manufacturing and good laboratory practice
- good manufacturing practice and process validation
- good regulatory practices
- hazards and safety management
- industrial pharmacy practice
- modern analytical techniques
- modern pharmaceutical analysis
- novel drug delivery system part-i
- novel drug delivery system-ii
- pharm. management -ii
- pharmaceutical analysis ii
- pharmaceutical and cosmetic analysis
- pharmaceutical formulation and development
- pharmaceutical formulation development and biopharmceutics
- pharmaceutical manufacturing technology
- pharmaceutical production management & technology
- pharmaceutical regulatory affairs
- pharmacological and toxicological screening methods-i
- pharmacological and toxicological screening methods-ii
- pharmacometrics and methods of biological evaluation of drugs
- pharmacotherapeutics
- principles of biopharmaceutics& pharmacokinetics
- product development and technology transfer
- quality control & quality assurance
- quality control and quality assurance
- quality management system
- regulatory affairs - i
- regulatory affairs and new drug applications
- regulatory aspects of hebbal and biologicals
- research methodology
- validation and product development