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CRITERION # | CRITERION | MEASURES INTENDED LEARNING OUTCOME(S) |
| | | 1 | Demonstrate ability to identify and resolve pharmaceutical issues related to the stability of pharmaceutical dosage forms. | LO1, LO2, LO3, LO4 | 2 | Evaluate the requirements needed to develop and validate chromatographic and biological assays and how such techniques can be applied to answer clinical questions. | LO1, LO2, LO3, LO4 |
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Assessment Task 3: Short answer question written online quiz |
Task Description: | Online Written quiz You will be required to complete 1 short answer written online quiz. The quiz will have between 10 and 15 questions. This activity will be conducted and supervised in Pharmacy Practice Room.
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Task Length: | |
Due Date: | Week 9 |
Weight: | 25 % |
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CRITERION # | CRITERION | MEASURES INTENDED LEARNING OUTCOME(S)
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| | | 1 | Describe scientific approaches to investigate the chemical stability and physical incompatibility of extemporaneous preparations. | LO2, LO3, LO4 | 2 | Demonstrate ability to identify critical methodological flows in an experimental design and formulate solutions to avoid identified issues. | LO2, LO3, LO4 | 3 | Demonstrate principles and applications of various laboratory techniques commonly used in pharmaceutical industries. | LO2, LO3, LO4 | 4 |
Through interpretation and analysis of the provided data, demonstrate the ability to determine the concentration of active pharmaceutical agents prepared through extemporaneous preparations. | LO2, LO3, LO4 |
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Assessment Task 4: Practical Exam |
Task Description: |
You will be assessed based on your competency in 1) applying chromatographic knowledge for the separation of analytes with different chemical structures; 2) determining the concentration of certain types of pharmaceuticals using a pre-validated analytical system; and 3) submission of experimental findings related to their practical assessment task. The duration of this supervised practical assessment (end of semester examination) will be of 2 hours. The weighting of observation component will be of 50% and submission of experimental findings will be of 50%. The practical assessment task in CSA743 will be more advanced than CSA741/CSA742 practical assessment tasks.
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Task Length: | |
Due Date: | Exam Period |
Weight: | 30 % |
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CRITERION # | CRITERION | MEASURES INTENDED LEARNING OUTCOME(S) |
| | | 1 | Demonstrate accuracy and completeness of dilution and pipetting skills. | LO2, LO3, LO4 | 2 |
Demonstrate ability to determine the concentration of certain types of pharmaceutical agents using a pre-validated analytical system. | LO2, LO3, LO4 | 3 | Demonstrate ability accurately interpret and analyse excremental findings | LO2, LO3, LO4 |
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