Medicines Verification v1.0.1
Full Capability status only. For this Capability, Solutions are required to meet all MUST EPICs and associated acceptance criteria.
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. |
C40E1 - 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
C40E2 - 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
C40E3 - 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:
- Interoperability Standard
- Overarching Standards
Roadmap
Suppliers will not be assessed or assured on these Roadmap Items as part of Onboarding