This industry-collaborated course offers students a unique opportunity to gain real-time, practical exposure to tablet formulation and quality evaluation, skills highly demanded in the pharmaceutical sector. Through hands-on training, expert-led sessions, and direct interaction with industry practices, learners develop strong technical competencies in tablet manufacturing, handling equipment, and performing essential QC tests. The course bridges the gap between academic knowledge and industrial requirements, enhances employability, and prepares students for roles in Production, QC/QA, and Formulation Development. It is an ideal choice for students aiming to build a solid foundation for a successful career in the pharma industry.This industry-collaborated course offers students a unique opportunity to gain real-time, practical exposure to tablet formulation and quality evaluation, skills highly demanded in the pharmaceutical sector. Through hands-on training, expert-led sessions, and direct interaction with industry practices, learners develop strong technical competencies in tablet manufacturing, handling equipment, and performing essential QC tests. The course bridges the gap between academic knowledge and industrial requirements, enhances employability, and prepares students for roles in Production, QC/QA, and Formulation Development. It is an ideal choice for students aiming to build a solid foundation for a successful career in the pharma industry.
What you'll learn
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CO-1.9 |
Understand the basics of different dosage forms, pharmaceutical incompatibilities and pharmaceutical calculations |
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CO-1.10 |
Understand the professional way of handling the prescription |
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CO-1.11 |
Preparation of various conventional dosage forms |
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CO-1.8 |
Know the history of profession of pharmacy |
01: Describe the fundamental principles of tablet formulation, excipient functions, and solid dosage form development.
02: Demonstrate hands-on skills in tablet manufacturing processes including granulation, blending, lubrication, and compression.
03: Operate essential tablet manufacturing and quality evaluation equipment such as compression machines, hardness testers, friability testers, disintegration and dissolution apparatus.
04: Perform and interpret key quality control tests including hardness, friability, weight variation, disintegration, and dissolution of tablets.
05: Apply Good Manufacturing Practices (GMP), safety procedures, and correct documentation while performing formulation and evaluation activities.
06: Identify common formulation challenges and utilize basic troubleshooting approaches used in industrial tablet development.
07: Prepare technical laboratory reports, maintain records, and communicate results effectively in line with industry expectations.
08: Integrate theoretical knowledge with practical skills to meet entry-level requirements for roles in Production, QC, QA, and Formulation & Development departments.
Sage Winter School (Sage University Indore)
Industrial Training on Tablet Formulation
1. What is the focus of the Industrial Training on Tablet Formulation?
This training focuses on providing hands-on knowledge of pharmaceutical tablet manufacturing processes, including granulation, compression, coating, quality testing, and regulatory requirements.
2. Who can enroll in this Winter School program?
Students pursuing B.Pharm, M.Pharm, D.Pharm, B.Sc. (Chemistry/Biotech), M.Sc. (Pharma/Science) or anyone interested in pharmaceutical manufacturing can enroll.
3. What skills will participants gain?
Participants will learn:
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Pre-formulation studies
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Granulation techniques (wet & dry)
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Tablet compression and tooling
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Tablet coating technologies
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In-process Quality Control (IPQC)
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GMP and industrial documentation
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Scale-up and troubleshooting
4. Is the training practical or theory-based?
The program combines both but is highly practical, with demonstrations of industrial equipment and exposure to real-time tablet formulation workflows.
5. Will students receive a certificate?
Yes. All participants receive an official Sage University Winter School Participation/Completion Certificate, useful for internships and placements.
6. What is the duration of the training?
The duration typically ranges from 1–2 weeks, depending on the batch schedule announced by the university.
7. Are there any prerequisites?
Basic knowledge of pharmaceutics or chemistry is helpful, but not mandatory.
8. What equipment or facilities will students experience?
Students may get exposure to:
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Rapid mixer granulator (RMG)
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Fluid bed dryer (FBD)
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Tablet compression machine
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Coating pan
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Hardness tester, friability tester, disintegration tester, dissolution apparatus
9. Is industrial/plant visit included?
Depending on availability, the program may include an industrial visit to a pharmaceutical manufacturing facility or in-house pilot plant training.
10. What career benefits does the training offer?
This training enhances readiness for roles in:
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Formulation R&D
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Production & manufacturing
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QA/QC
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Regulatory affairs
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Pharmaceutical sales & technical support
11. How can students register?
Students can register through the Sage University official website, training & placement cell, or the Department of Pharmacy.
12. Is there a fee for the Winter School program?
Yes, a nominal fee is typically applicable. The exact amount is shared by the university during registration.
13. Do participants receive study material?
Yes. Modules, SOPs, and training notes on tablet formulation are provided.
14. Will there be assessments or projects?
Some batches include small assessments, hands-on tasks, or mini-projects related to formulation development.
15. Whom can students contact for more details?
Students can reach out to the Department of Pharmaceutical Sciences or the Winter School coordinator for detailed schedules and registration support.
