Description
Supports compliance with the Falsified Medicines Directive and minimise the risk that falsified medicinal products are supplied to the public.
Outcomes
For General Practice: | Minimise the risk that falsified medicinal products are supplied to the public. |
Epic 1 - verify Medicinal Product Unique Identifiers
As 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 Identifiers
Given 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 public
Given 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
Epic 2 - decommission Medicinal Products
As a Practice User
I want to decommission Medicinal Products
So that Medicinal Products are decommissioned
Acceptance criterion 1: decommission Medicinal Products
Given 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
Epic 3 - record the integrity of Anti-tampering Devices
As 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 Devices
Given 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:
Roadmap
Suppliers will not be assessed or assured on these Roadmap Items as part of Onboarding