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Supports compliance with the Falsified Medicines Directive and minimise the risk that falsified medicinal products are supplied to the public. |
For General Practice: | Minimise the risk that falsified medicinal products are supplied to the public. |
C40E1 - verify Medicinal Product Unique IdentifiersAs a Practice User I want to verify Medicinal Product Unique Identifiers So that the Medicinal Product Unique Identifiers are verified Acceptance criterion 1: verify Medicinal Product Unique IdentifiersGiven the Practice User is permitted to verify Medicinal Product Unique Identifiers When the Practice User chooses to verify a Medicinal Product Unique Identifier And the authenticity of Medicinal Product Unique Identifier is verified Then the Medicinal Product Unique Identifier is verified Acceptance criterion 2: fail to verify Medicinal Products for supply to the publicGiven the Practice User is permitted to verify Medicinal Product Unique Identifiers When the Practice User chooses to verify a Medicinal Product Unique Identifier And the authenticity of Medicinal Product Unique Identifier is not verified Then the Medicinal Product Unique Identifier is not verified C40E2 - decommission Medicinal ProductsAs a Practice User I want to decommission Medicinal Products So that Medicinal Products are decommissioned Acceptance criterion 1: decommission Medicinal ProductsGiven the Practice User is permitted to decommission Medicinal Products When the Practice User chooses to decommission a Medicinal Product And the integrity of the Anti-tampering Device is not compromised And the authenticity of Medicinal Product Unique Identifier is verified Then the Medicinal Product is decommissioned |
C40E3 - record the integrity of Anti-tampering DevicesAs a Practice User I want to record the integrity of Anti-tampering Devices So that the integrity of Anti-tampering Devices is recorded Acceptance criterion 1: record the integrity of Anti-tampering DevicesGiven the Practice User is permitted to record the integrity of Anti-tampering Devices When the Practice User chooses to record the integrity of an Anti-tampering Device Then the integrity of the Anti-tampering Device is recorded |
Suppliers will have to attain compliance with these Standards during the compliance stage before they can be live on a framework with this Capability: None |
Suppliers will have to attain compliance with these Standards during the compliance stage before they can be live on a framework with this Capability:
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Suppliers will not be assessed or assured on these Roadmap Items as part of Onboarding |