Supports compliance with the Falsified Medicines Directive and 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

Suppliers will not be assessed or assured on these Roadmap Items as part of Onboarding