記録された日時: March 19 2014
Duration: 51 minutes 30 secondsThe end point of any particle size measurement is to provide improved product or process understanding and/or control. It order to achieve this, it is important that the size specifications selected are relevant to those products or processes. In this webinar, we will look at the size distribution data generated by technqiues such as laser diffraction and image analysis, and will consider how these can be used to generate realistic product specifications.
Table of contents
1. Setting pharmaceutical product specifications for particle size analysis
2. Setting pharmaceutical product specifications for particle size analysis
3. What should be the first stage in setting a specification?
4. The first stage in QbD is definition of the target product profile and its associated quality attributes
5. When should particle size be considered as a critical quality attribute?
6. Where should I measure my product?
7. When should I measure my product?
8. What product form is most relevant?
9. Dissolution dynamics: what should I measure?
10. Content uniformity: what should I measure?
11. Dispersion stability: what should I measure?
12. Suspension properties : what should I measure?
13. Case study: setting specifications for solid dosage forms
14. Selecting appropriate control parameters
15. Setting specification tolerances
16. Controlling the dispersion properties of powders
17. Controlling the dispersion properties of powders
18. Optimising atomisation processes
19. Optimising atomisation processes
20. Optimising atomisation processes
21. Optimising atomisation processes
22. Setting specifications for specific components within pharmaceutical blends
23. Setting specifications for specific components within pharmaceutical blends
24. Linking measurements specifications and product manufacturing specification
25. Setting specifications: tablets
27. Contact Information