Master - Professional Master in Pharmaceutical Industry - Pharmaceutics and Industrial Pharmacy
| Course ID | Course Name | Credit 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 | |