Master - Professional Master in Pharmaceutical Industry
| Course Code | Course Name | Exam. Hours | Exam. Hours | Exam. Marks | Semester | Mandatory/Elective |
|
PM101
|
Pharmaceutical development of generic and brand roducts
|
[2+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM102
|
Stability testing of pharmaceutical dosage forms and drug substances
|
[1+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM103
|
Specification, Test procedure and acceptance criteria
|
[1+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM104
|
Biowaiver & bioequivalence studies for generic products
|
[2+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM105
|
Analytical development procedures & Validation of Analytical methods
|
[2+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM106
|
The regulatory system & regulatory standards of re ulator authorities
|
[2+0]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM107
|
Basics of pharmaceutical statistics
|
[1+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM108
|
Good laboratory practice (GLP) & laboratory control
|
[2+1]
|
3
|
0
|
Semester One
|
Mandatory
|
|
PM109
|
Impurities of drug substance & drug products
|
[1+1]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM110
|
Product scaling-up & technology transfer
|
[1+1]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM111
|
Application of Clinical trials for development of brand products
|
[2+0]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM112
|
Common technical document (CTD) of pharmaceutical products
|
[1+1]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM113
|
Good manufacturing practices (GMP) guidelines (part 1)
|
[1+1]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM114
|
Pharmaceutical manufacturing technoloies of drug products
|
[2+0]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM115
|
Application of ICH safety guidelines
|
[1+1]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM116
|
Research project
|
[2+0]
|
0
|
0
|
Semester Two
|
Mandatory
|
|
PM117
|
Good manufacturing practices (GMP) gidlines (part 2)
|
[1+1]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM118
|
Environment, health, & safety standards
|
[1+1]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM119
|
Application of Pharmacopoeias in harmaceutical industries
|
[1+1]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM120
|
Validations systems
|
[2+0]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM121
|
Good Design Practices for (GMP) Pharmaceutical Facilities (part 1)
|
[2+1]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM122
|
Continuous manufacturing & pharmaceutical product lifecycle management
|
[1+1]
|
0
|
0
|
Semester Three
|
Mandatory
|
|
PM123
|
Good Design Practices for GMP Pharmaceutical Facilities (part 2)
|
[2+1]
|
0
|
0
|
Semester Four
|
Mandatory
|
|
PM124
|
GMP guide for active pharmaceutical ingredients Q7
|
[2+0]
|
0
|
0
|
Semester Four
|
Mandatory
|
|
PM125
|
Information & data management system
|
[1+1]
|
0
|
0
|
Semester Four
|
Mandatory
|
|
PM126
|
Supply chain and distribution management
|
[1+1]
|
0
|
0
|
Semester Four
|
Mandatory
|
|
PM127
|
Strategic and operational management
|
[1+1]
|
0
|
0
|
Semester Four
|
Mandatory
|
|
2005
|
Critical Thinking - University Requirements
|
--
|
0
|
0
|
Semester Four
|
Mandatory
|
|
PM128
|
Research and development R&D Methodology
|
6
|
0
|
0
|
Training
|
|
|
PM129
|
Quality control QC professional
|
6
|
0
|
0
|
Training
|
|
|
PM130
|
Quality assurance Quality control & GMP compliance
|
6
|
0
|
0
|
Training
|
|
|
PM131
|
Pharmaceutical Production GMP compliance
|
6
|
0
|
0
|
Training
|
|
|
PM132
|
Planning & supply chain Pharmaceutical Production
|
6
|
0
|
0
|
Training
|
|
|
PM133
|
Regulatory affairs Quality assurance
|
6
|
0
|
0
|
Training
|
|