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The representation of a medicinal product as it is supplied in a package by a by a single organisation (manufacturer or supplier) in a single jurisdiction under a single name (which may be a trade or brand name) for placement into the supply chain. It is a subtype of and real world equivalent to the Packaged Clinical Drug (PCD ) class described above.
Use
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Cases
The following use cases are supported by the Real Packaged Clinical Drug concept class:
- Describing medication process activities: prescribing, dispensing, administration and medication statements; of these, dispensing and administration will use this concept when it is available to clearly state which actual packaged product (or content from it) was used/supplied to the patient (with batch/lot and expiry information if required, either manually or by automatic identification and data capture (AIDC) - for example scanning the bar code on the package)
- Compliance monitoring, using pack size information to calculate whether a patient is following the dosage instructions correctly (how quickly a repeat supply of a package of medication is required)
- Anti-counterfeiting: in support of initiatives such as the Falsified Medicines Directive (see amended Directive 2001/83/EC) using AIDC and which requires scanning of medicines at the point of supply (to the patient)
- Reimbursement: national or local systems may set pricing or eligibility against actual packaged products
- Pharmacovigilance – especially for product defects and labelling issues
- The association between the clinical representation of medicinal products and their representation in the supply chain for supply chain management
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National extensions that require real packaged clinical drug concepts can are advised to define their RPCD real packaged clinical drug concepts using real clinical drug concepts from their national extension or, if only real packaged clinical drug concepts are authored without RCDs, using clinical drugs from the international edition or national extension. However, if real packaged clinical drug concepts are authored without RCDs, there is little opportunity for grouping of concepts on the right-hand/real side of the model; although real packaged clinical drug concepts with the same product name and supplier would have the required attributes to group them together, there is no parent grouper concept to place them under, so the grouping would be hard to show. If real packaged clinical drug concepts without RCDs and without PCDs, then the stated and inferred views will be equivalent, there will be no grouping concepts for the real packaged clinical drug concepts to be associated with.. This allows grouping of package concepts with their associated real clinical drug using the "contains clinical drug" value and information from that (for example, excipient information) can be transferred through that composition relationship if required.
Existing national terminology equivalents:
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Gliffy Diagram macroId 837f09bd-23cf-4695-a860-decb2b9cc508 displayName RPCD Template Gliffy name RPCD Template Gliffy pagePin 12
Figure 34: Template for a simple real packaged clinical drug
Example: simple real packaged clinical drug
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: stated view followed by the inferred view
Figure 35: Example of a real packaged clinical drug described using a real clinical drug - stated view
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Figure 36: Example of a real packaged clinical drug described using a real clinical drug - inferred view
Example: simple real packaged clinical drug described using clinical drug: stated view followed by the inferred view
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Figure 37: Example of a real packaged clinical drug described using a clinical drug - stated view
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Figure 38: Example of a real packaged clinical drug described using a clinical drug - inferred view
Optional Additional Information
The following information may be additionally used to describe the Real Packaged Clinical Drug concept in a national extension. With the exception of container information, the attribute concepts and values to populate these, if this data is to be held in a structured form, would need to be authored into the extension using reference sets.
Optional Additional Information
As with the real clinical drugs, national extensions may require additional information to be associated with real packaged clinical drugs. This may include characteristics of the packaged product that can be described within the SNOMED CT structure using attributes and values, managed alongside the SNOMED CT structure (e.g. in a reference set) and/or relationships between identification systems should be managed in cross maps.
- Packaged product characteristics may include package/container types Package/container type (e.g. bottle, box, jar, tube ); some use cases may also require information about sterile wrapping of some medicinal product packaging
- License information - for those jurisdictions that license at a package level rather than at the real clinical drug level
- License identification ("authorisation number")
- Licensing class and/or legal status of supply
- Usage information (prescribability within a particular jurisdictional context) including legal status
- Reimbursement information
- Administration - to support various use cases including robotic dispensing) and administration device supplied in the package (e.g. medicine spoon, vaginal applicator, applicator brush for cutaneous liquid products)
- Knowledge about the product may include usage information such as availability within the supply chain, licensing/authorization category and/or legal status of supply, and prescribability information including reimbursement categories.
- Other identification systems for a real packaged clinical drug may include licensing/authorization number, if this is provided for individual packages or Global Trade Identification Number
In jurisdictions where repackaging and/or "parallel importing" are authorised, a national extension may wish to consider having a relationship between the repackaged or parallel imported real packaged clinical drug and the real clinical drug supplied by the original manufacturer, if that is present within the jurisdiction.
IDMP Compatibility
This concept as defined is equivalent to the Packaged Medicinal Product of ISO 11615, which in that standard is identified by a PCID. As the representation of the "real world product" authorised for sale and/or supply that exists for all jurisdictions and which is marketed into the supply chain for use, it is the concept that should form the 1:1 join between representation in the regulatory domain (IDMP) and representation in the clinical domain (SNOMED CT and national medicinal product terminologies), even if some national medicinal product terminologies choose not to represent it, but only an abstraction of it (i.e. the Real Clinical Drug class of concepts).
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