MASTER OF PHARMACEUTICAL LEGISLATION AND REGULATORY CONTROL (COURSEWORK)
MASTER OF PHARMACEUTICAL LEGISLATION AND REGULATORY CONTROL.
Programme Overview
The Masters in Pharmaceutical Legislation and Regulatory Control (PLRC) is a mode course one (1) year program with the aim of producing knowledgeable graduates in pharmaceutical legislation and regulatory affairs to meet the demand by government health related regulatory bodies and health related industries, such as pharmaceutical, cosmeceutical and nutraceutical.
Full-Time Duration: 2 Semesters + 1 Special Semester, (Coursework)
Part-Time Duration: 4 Semesters + 2 Special Semester, (Coursework)
Programme Structure
Core Courses (21 credits)
Pharmaceutical Legislation
Introduction to Legislation Writing and Auditing
Quality Assurance
Pharmaceutical Product Development
Pharmaceutical Analysis and Testing
Research Methodology
Elective Courses (9 credits) - 3 only
Pharmaceutical Bioinformatics
Advance Medicinal Chemistry
Pharmacogenomics, Pharmacokinetics, Pharmacodynamics in Precision Medicine
Design of Pharmaceutical Dosage Forms
Development of Novel Drug Delivery Systems
Pharmaceutical Engineering and Production Facilities