| Relate unique and essential central core concepts. |
|
|
|
|
|
| Review regulatory framework requirements. |
|
|
|
|
|
| Explain standards of practice for non-hazardous and hazardous drug compounding. |
|
|
|
|
|
| Describe components of a standard operating procedure. |
|
|
|
|
|
| Discuss business, marketing, and sales for a successful practice. |
|
|
|
|
|
| Explain characteristics for routes of delivery in non-sterile compounding. |
|
|
|
|
|
| Describe the chemical composition of different dosage forms. |
|
|
|
|
|
| Solve pharmaceutical calculations in compounding. |
|
|
|
|
|
| Match excipients to dosage forms, chemical composition, and routes of delivery. |
|
|
|
|
|
| Match base types to dosage forms, chemical composition, and routes of delivery. |
|
|
|
|
|
| Relate drug monographs and certificates of analysis to compounding. |
|
|
|
|
|
| Describe techniques and technology used during compounding. |
|
|
|
|
|
| Outline the components of process development. |
|
|
|
|
|
| Demonstrate the use of a master formulation record. |
|
|
|
|
|
| Discuss the requirements of a compounding record. |
|
|
|
|
|