Pharm (Pharmacology)
Intake: 15 Seats
Postgraduate students in Pharmacology at SIPS are immersed in a research-driven academic environment focused on developing a strong foundation in drug action, safety, and efficacy. The Department of Pharmacology offers a well-structured and dynamic curriculum that blends essential pharmacological concepts with advanced laboratory competencies.
This program equips students with a deep understanding of pharmacokinetics, pharmacodynamics, and systemic pharmacology, while also exploring molecular mechanisms of drug action. Students receive extensive hands-on training in preclinical screening, toxicological evaluation, and drug development processes.
Through integrated modules in cell biology, immunology, and pharmacogenomics, learners gain exposure to modern tools and approaches in pharmacological research. Our experienced faculty, actively involved in both teaching and research, mentor students to become skilled pharmacologists for careers in academia, pharmaceutical industry, and research institutes.
Key Features:
- Advanced Pharmacology and Toxicology Laboratories for in vivo and in vitro studies
- Training in Laboratory Animal Handling, CPCSEA guidelines, and GLP compliance
- Access to leading e-resources and international journals in Experimental Pharmacology
- Faculty-guided research projects in pharmacogenomics, cell signaling, and molecular biology
- Hands-on exposure to flow cytometry, ELISA, Western blotting, PCR, and related techniques
M. Pharm (Regulatory Affairs)
Intake: 15 Seats
The M. Pharm in Regulatory Affairs at SIPS is a specialized program designed to produce skilled professionals capable of navigating the complex global regulatory landscape of the pharmaceutical industry. The course emphasizes regulatory compliance, international guidelines, documentation standards, and the drug approval process.
Students are trained in advanced pharmaceutical analysis, regulatory documentation, and dossier compilation, including DMFs, CTD/eCTD, and stability studies. The curriculum integrates core aspects of drug development, safety evaluation, and clinical trial regulation, with emphasis on international standards such as ICH, USFDA, EMA, TGA, and WHO.
Graduates of this program acquire both theoretical knowledge and practical expertise needed for regulatory submissions, clinical trial documentation, pharmacovigilance, and post-marketing surveillance. This course aims to develop professionals who uphold product quality, safety, and efficacy in accordance with global regulatory standards.
Key Features:
- Advanced Analytical Instrumentation Laboratory with modern equipment
- In-depth training in Regulatory Submissions: NDA, ANDA, IND, IMPD
- Comprehensive understanding of global regulatory frameworks
- Curriculum aligned with current industry standards and pharmacovigilance practices
- Hands-on experience with CTD/eCTD compilation, BA/BE studies, and interactions with CROs
- Frequent seminars and workshops on GMP, documentation standards, and regulatory compliance
M.Pharm: (Pharmaceutics)
Intake: 15 Seats
Postgraduates at the SIPS benefit from the same high teaching standards as their undergraduate counterparts. The Department of Pharmaceutics at SIPS offers post graduate students the opportunity to pursue a program of study that is directed towards meeting the individual career objectives in the area of pharmaceutical expertise. Students are provided with one of the most dynamic programs in the area of pharmaceutical product discovery and development. Qualified & dedicated faculty members of this department are always keen to show their talents by way of technical lectures, innovations in teaching and tutorials for making skilled, better and effective practical knowledgeable pharmaceutical technologists in order to build up good citizens in future. Salient Features State-of-the-art well equipped Laboratories Computer Center with 24 Hours Internet facility Class Rooms with LCD Projectors Library facility rich with technical/ nontechnical literature. To cater the PG students, college library has plenty of reference books, textbooks and handbooks required for teaching & learning activities. Besides technical books there are 25 National & 12 International journals, magazines & 93 e-journal subscriptions like Science Direct, Elsevier & Bentham Science series.
M. Pharm (Quality Assurance)
Intake : 15 Seats
“Quality assurance” is a wide ranging concept covering all matters that individually or collectively influence the quality of a product. It is the totality of the arrangements made with the object of ensuring that pharmaceutical products are of the quality required for their intended use. Quality assurance therefore incorporates GMP and other factors, including those outside the scope of this guide such as product design and development.
A programme particularly intended to create professionals who will make a evidence in the pharmaceutical industry by assuring the quality of the pharmaceutical product.
In nutshell Quality assurance deals with Identity, Strength, Safety, Purity and Efficacy of product.
Quality assurance provides wide career opportunities in different areas of pharmaceutical fields