Course Content
Drug Good Manufacturing Practices Health Canada Parameters
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Before Starting
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Module One: Prerequisite Information (1)
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Module One: Prerequisite Information (2)
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Module Two: Premises (C.02.004)
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Module Two: Equipment (C.02.005)
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Module Three: Personnel (C.02.006)
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Module Four: Sanaitation – Premises (C.02.007)
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Sanitation – Employees (C.02.008)
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Module Five: Raw Material Testing (C.02.009)
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Raw Materials Testing(C.02.010)
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Module Six: Manufacturing Control (C.02.011 and C.02.012) – 1
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Module Six: Manufacturing Control (C.02.011 and C.02.012) – 2
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Module Six: Manufacturing Control(C.02.011 and C.02.012) – 3
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Module Six: Manufacturing Control (C.02.011 and C.02.012) – 4
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Manufacturing Control (C.02.012) – 1
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Manufacturing Control (C.02.012) – 2
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Module Seven: Quality Control Department (C.02.013, 014 & 015)
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Quality Control Department Operational Responsibilities
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Lab Testing
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Module Eight: Packaging Material Testing (C.02.016)
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Packaging Material Testing (C.02.017)
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Module Nine: Finished Product Testing (C.02.018)
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Finished Product Testing (C.02.019) – 1
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Finished Product Testing (C.02.019) – 2
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Module Ten: Records (C.02.020, C.02.021, C.02.022, C.02.023 and C.02.024) – 1
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Module Ten: Records (C.02.020, C.02.021, C.02.022, C.02.023 and C.02.024) – 2
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Module Eleven: Samples (C.02.025 and C.02.026)
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Module Twelve: Stability (C.02.027)
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Module Twelve: Stability (C.02.028)
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✅ Checklists – Stability – Potency
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✅ Checklists – Stability – Purity
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✅ Checklists – Stability – Physical Characteristics
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Sterile Products (C.02.029)
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Course Completion
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