Pharmaceutical Dosage Forms I (Practical)

List of Practicals

1. 12 experiments must be performed)
2. Preformulation study of any drug/excipient as per pharmacopoeia.
3. Evaluation of powder flow properties for tablet blends.
4. Evaluation of effect of lubricating agents on powder flow properties.
5. Preparation and evaluation of tablets by dry granulation.
6. Preparation and evaluation of tablets by wet granulation.
7. Quality control of marketed tablets (IR, coated, enteric-coated).
8. Preparation and evaluation of coated tablets.
9. Comparison of dissolution profiles of marketed preparations.
10. Preparation and evaluation of hard-/non-gelatin capsules (fill weight, disintegration).
11. Virtual demonstration: hard-gelatin shell and soft-gel manufacturing (with of aseptic line/isolator).
12. Evaluation of packaging materials: primary and secondary/tertiary.
13. Preparation and evaluation of sustained-release tablets.
14. Preparation and evaluation of enteric-coated tablets.