Dosage Form Design Parameters

<p>1. Levels of solid state properties: Role of different levels during pharmaceutical development<br>2. Polymorphism and its Implications in Pharmaceutical Product Development<br>3. Basics of crystallization process applied in drug research<br>4. Role of amorphous state in drug delivery<br>5. Particulate level properties and its implications on product performance and processing<br>6. Bulk level properties and its role in formulation development and processing<br>7. Concepts of hypothesis testing and types of errors<br>8. Experimental design and analysis of variance<br>9. Basic concept and application of Sampling procedures<br>10. Statistical techniques in Pharmaceutical Product Development<br>11. Drug-excipient interaction and incompatibilities<br>12. Documentation protocols in product development department including clinical records<br>13. Correlation between in-vitro and in-vivo screens: Special emphasis on high throughput screening, high throughput pharmacokinetic analysis<br>14. Sterilization of pharmaceuticals: Technology, Equipment and Validation<br>15. Package development of pharmaceutical products: Aspects of packaging materials used for Pharmaceutical Products<br>16. Package types for different dosage forms<br>17. Food and drug laws effecting pharmaceutical product design, development and commercial manufacturing<br>18. Guiding Principles for Human and Animal Research during pharmaceutical product development<br>19. Applications of Computer in Pharmaceutical Product Development<br>20. Patents and other intellectual property rights in drug delivery<br>21. Computer Aided Prediction of Pharmacokinetic (ADMET) Properties<br>22. Ethics and Legal Protection of Uses of Computer Applications in Pharmaceutical Research</p>