Dosage Form Design Parameters

1. Levels of solid state properties: Role of different levels during pharmaceutical development2. Polymorphism and its Implications in Pharmaceutical Product Development3. Basics of crystallization process applied in drug research4. Role of amorphous state in drug delivery5. Particulate level properties and its implications on product performance and processing6. Bulk level properties and its role in formulation development and processing7. Concepts of hypothesis testing and types of errors8. Experimental design and analysis of variance9. Basic concept and application of Sampling procedures10. Statistical techniques in Pharmaceutical Product Development11. Drug-excipient interaction and incompatibilities12. Documentation protocols in product development department including clinical records13. Correlation between in-vitro and in-vivo screens: Special emphasis on high throughput screening, high throughput pharmacokinetic analysis14. Sterilization of pharmaceuticals: Technology, Equipment and Validation15. Package development of pharmaceutical products: Aspects of packaging materials used for Pharmaceutical Products16. Package types for different dosage forms17. Food and drug laws effecting pharmaceutical product design, development and commercial manufacturing18. Guiding Principles for Human and Animal Research during pharmaceutical product development19. Applications of Computer in Pharmaceutical Product Development20. Patents and other intellectual property rights in drug delivery21. Computer Aided Prediction of Pharmacokinetic (ADMET) Properties22. Ethics and Legal Protection of Uses of Computer Applications in Pharmaceutical Research