Exam Details
| Subject | computer aided drug delivery system | |
| Paper | ||
| Exam / Course | m.pharm. pharmaceutics | |
| Department | ||
| Organization | solapur university | |
| Position | ||
| Exam Date | December, 2018 | |
| City, State | maharashtra, solapur |
Question Paper
Master of Pharmacy (Semester II) (New CBCS) Examination, 2018
pharmaceutics
Computer Aided Drug Delivery System
Day and Date Thursday, 13-12-2018 Max. Marks 75
Time 10.30 a.m. to 1.30 p.m.
I. Answer any five questions
Give an overview of use of computers in pharmaceutical drug development.
Explain pharmaceutical automation and its advantages and disadvantages in
drug development.
Discuss the common issues in computer ethics in pharmaceutical research.
Explain the uses of computers in development of pharmaceutical emulsions.
Discuss factors to be considered while selecting data collection and
management system for clinical trials.
Explain the provision for legal protection of innovative uses of computers
in research and development.
II. Answer any three questions (3×10=30)
Explain computer simulation in PK/PD using whole organism.
Discuss various in vitro dissolution and in vitro-in vivo correlations used
during pharmaceutical development.
Describe computer aided formulation development by factorial design.
Explain computational modeling of drug absorption and excretion.
III. Discuss in detail the concepts of Quality-by-Design with respect to ICH Q8
guideline.
pharmaceutics
Computer Aided Drug Delivery System
Day and Date Thursday, 13-12-2018 Max. Marks 75
Time 10.30 a.m. to 1.30 p.m.
I. Answer any five questions
Give an overview of use of computers in pharmaceutical drug development.
Explain pharmaceutical automation and its advantages and disadvantages in
drug development.
Discuss the common issues in computer ethics in pharmaceutical research.
Explain the uses of computers in development of pharmaceutical emulsions.
Discuss factors to be considered while selecting data collection and
management system for clinical trials.
Explain the provision for legal protection of innovative uses of computers
in research and development.
II. Answer any three questions (3×10=30)
Explain computer simulation in PK/PD using whole organism.
Discuss various in vitro dissolution and in vitro-in vivo correlations used
during pharmaceutical development.
Describe computer aided formulation development by factorial design.
Explain computational modeling of drug absorption and excretion.
III. Discuss in detail the concepts of Quality-by-Design with respect to ICH Q8
guideline.
Other Question Papers
Subjects
- advanced biopharmaceutics and pharmacokinetics
- advanced pharmaceutical analysis (old)
- advanced pharmaceutical chemistry – i (old)
- advanced pharmaceutical chemistry – ii
- advanced pharmaceutical chemistry – iii (old) (cgpa/cbcs)
- advanced pharmaceutics – ii
- advanced pharmaceutics – iii (old)
- advances in drug delivery (old)
- audits and regulatory compliance
- computer aided drug delivery system
- cosmeticology (elective)
- cosmetics and cosmeceutica
- cosmetics and cosmeceuticals
- drug delivery system
- drug design (elective) (old)
- elective : quality control (old)
- hazards and safety management
- modern pharmaceutical analytical technique
- modern pharmaceutical analytical techniques
- modern pharmaceutics
- molecular pharmaceutics (nano tech and targeted dds)
- pharmaceutical manufacturing technology
- pharmaceutical validation
- pharmaceutics (biopharmaceutics and pharmacokinetics(old) (elective)
- product development (elective)(old)
- product development and technology transfer
- quality assurance
- quality assurance techniques – i
- quality assurance techniques – ii (old)
- quality assurance techniques – iii
- quality control (old)
- quality control and quality assurance
- quality management system
- regulatory affairs
- sterile product formulation and technology
- sterile product formulation and technology (old) (elective)
- therapeutic drug monitoring (old) (elective)