Identify elements of the current regulatory framework for compounding in Canada as it applies to Federal, Provincial/Territorial jurisdictional law, and standards of practice. |
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Describe quality assurance, risk management, and verification program requirements outlined in the Guidance Document for Pharmacy Compounding of Non-sterile Preparations. |
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Identify policy and procedure requirements that reflect the current NAPRA model standards. |
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Detail current requirements of master formulation and compounding records. |
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Discuss approaches to ensure personnel safety, and the quality and safety of non-sterile preparations. |
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Apply and adapt standards of practice to best suit your compounding practice. |
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Demonstrate the application and integration of a learned policy and procedure infrastructure into your practice. |
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Differentiate competency assessments from compliance indicators. |
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Integrate a best practice’s approach commensurate with the size, complexity, and risks associated specifically to your compounding practice. |
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Develop a strategic action plan to manage the implementation of the new 2018 NAPRA standards of practice. |
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