Department of Pharmaceutical Chemistry and Quality assurance

The Department of Pharmaceutical Chemistry, Quality Assurance, and Pharmaceutical Analysis offer a comprehensive educational experience through a well-rounded curriculum for both undergraduate and postgraduate students. Our programs feature meticulously designed lectures and hands-on laboratory sessions that integrate theoretical knowledge with practical application. This structure ensures that students not only grasp fundamental concepts but also acquire the skills needed to address real-world industry challenges effectively. Our extensive syllabus and immersive learning approach bridge the gap between theory and practice, preparing students to excel in their professional careers.

Pharmaceutical Chemistry serves as the foundation for grasping essential principles in life and health sciences. Our undergraduate program emphasizes a diverse range of subjects, including biochemistry, inorganic chemistry, organic chemistry, pharmaceutical medicinal chemistry, computer-aided drug design, and pharmaceutical analysis. This comprehensive curriculum equips students with a solid understanding of chemical processes and their applications, providing a crucial basis for further exploration in the field and preparing them for advanced study and professional practice.

The Quality Assurance specialization prepares students to excel in analytical, regulatory, and quality roles within the pharmaceutical and related industries, all within a GLP-compliant framework. The course is meticulously crafted to provide a thorough understanding of quality management principles and systems employed in manufacturing. It covers essential topics such as current Good Manufacturing Practices (cGMP), stability testing of drug substances and products, statistical quality approaches, hazard assessment, equipment qualification, Quality by Design (QbD), and Process Analytical Technology (PAT). This specialization ensures that students gain both theoretical knowledge and practical skills to effectively contribute to quality assurance and regulatory compliance in the pharmaceutical sector.

Thrust Area:

• CADD, Insilico Molecular Modelling

• Green Synthesis- Microwave assisted synthesis

• Calibration and Validation of Equipment

• Bioanalytical Method Development and Validation

• Documentation