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Administrable Pharmaceutical Dose Form.

This code represents the form of the medication (e.g. tablet, capsule, liquid.html)

Since the EDQM Standards Terms, together with UCUM, is one of the IDMP terminologies actually available for usage, this code system has been selected  as referecne terminology for representing Pharmaceutical Dose forms;Pakages and Route of Administration.

It is known that also alternative jurisdictional and international terminologies are known to be used for this concept domain, as NCI or SNOMED CT.

This structure describes the packaging of the medication.

The <formCode> element provides the code for the particular package.

If the package has a brand name, it can be described in the <name> element.

The <capacityQuantity> element describes the capacity of the packaging, while the <quantity> the actual quantity of inner packaged items in the outer packaging container. The product might have a single (30 pills bottle.html) or multiple (5 vials 10 ml; box with 2 blisters of 20 tablets.html) layers of packaging.

In the latter case, the most inner (nested.html) item represents the most outer package item.

For example the case 

  --Box 

  -----2 blisters 

  --------20 tablets 

is described as "20 tablets" contained by "a blister"; "2 blisters" contained by one box.

The most inner package represents the Packaged Medicinal Product.

When the IDMP Packaged Medicinal Product ID (PCID.html) will become actually available for usage, the most inner package <code> element will be used to convey the IDMP PCID.

The quantity which specified how many inner packaged content entities are in an outer packaging container entity.

It represents the most inner Package Item or the Packaged Medicinal Product.

If this is also the most outer <containerPackagedProduct> than the <code> element can be used to convey the (IDMP.html) Packaged Medicinal Product ID (e.g. the IDMP PCID when it will become actually available for usage.html).  

The presence of the PCID indicates that that element represents the "Packaged Medicinal Product".

It represents the Name of the Package Item or of the Packaged Medicinal Product.

If this is also the most outer <containerPackagedProduct> than this element can be used for the brand name.

This element encodes the type of the most inner package item or of the or the Packaged Medicinal Product.

Since the EDQM Standards Terms, together with UCUM, is one of the IDMP terminologies actually available for usage, this code system has been selected  as referecne terminology for representing Pharmaceutical Dose forms; Packages and Route of Administration.

It represents the functional capacity of the container: e.g. bottle containing up to 20 tablets or ampule of 10 ml.

In case of multiple layers of packaging (5 vials 10 ml; box with 2 blisters of 20 tablets.html) this element can be used for describing the intermediate Packaged Medicinal Product Item or the Packaged Medicinal Product.

For example in the case 

  --Box 

  -----2 blisters 

  --------20 tablets 

it describes the "2 blisters" 

In the case of 

  --Box 

  -----5 vials

it represents the Packaged Medicinal Product. 

The quantity which specified how many inner packaged content entities are in an outer packaging container entity.

It represents the intermediate Package Item or the Packaged Medicinal Product

If this is also the most inner  <containerPackagedProduct> than the <code> element can be used to convey the (IDMP.html) Packaged Medicinal Product ID (e.g. the IDMP PCID when it will become actually available for usage.html).  

The presence of the PCID indicates that that element represents the "Packaged Medicinal Product".

It represents the Name of the Package Item or of the Packaged Medicinal Product

If this is also the most inner  <containerPackagedProduct> than this element can be used for the brand name.

This element encodes the type of the most inner package item or of the or the Packaged Medicinal Product.

Since the EDQM Standards Terms, together with UCUM, is one of the IDMP terminologies actually available for usage, this code system has been selected  as reference terminology for representing Pharmaceutical Dose forms; Packages and Route of Administration.

It represents the functional capacity of the container: e.g. bottle containing up to 20 tablets or ampule of 10 ml.

In case of multiple layers of packaging (box with 2 blisters of 20 tablets.html) this element is used for describing the most outer Packaged Medicinal Product Item or the Packaged Medicinal Product.

For example in the case 

  --Box 

  -----2 blisters 

  --------20 tablets 

it describes the Packaged Medicinal Product. 

The quantity which specified how many inner packaged content entities are in an outer packaging container entity.

When present, it represents the Packaged Medicinal Product

When present, it can be used to convey the (IDMP.html) Packaged Medicinal Product ID (e.g. the IDMP PCID when it will become actually available for usage.html).

When present, it can be used for the representing the brand name.

When present, it encodes the type of the outer package.

Since the EDQM Standards Terms, together with UCUM, is one of the IDMP terminologies actually available for usage, this code system has been selected  as referecne terminology for representing Pharmaceutical Dose forms; Packages and Route of Administration.

It represents the functional capacity of the container: e.g. bottle containing up to 20 tablets or ampule of 10 ml.

This module is used for representing the classification of the Substance according to the WHO Anatomical Therapeutic Chemical (ATC.html) Classification System.

The classCode of "GRIC" identifies this structure as the representation of a generic equivalent of the medication described in the current Medicine entry.

The element contains the ATC code of this medicine.

The Medicinal Product can be classified according to various classification systems, which may be jurisdictional or international. The classification system itself is specified using an appropriate identification system; the controlled term and the controlled term identifier shall be specified.

When the IDMP Pharmaceutical Product Identifier(s.html) (PhPID Set.html) will become actually available for use, the PhPID will be represented by the generalizedMaterialKind/code element.

When the IDMP Pharmaceutical Product Identifier(s.html) (PhPID Set.html) will become actually available for use, this element will be used for representing the IDMP PhP Id.

The level and the stratum of the PhPID will be distiguished by the OID of the code system.

This module provides the list of the ingredients (substances with a role.html) used for this product; one or more ingredients may be present.

The classCode of "ACTI" indicates that this is an active ingredient.

The medication strength is represented as the ratio of the active ingredient(s.html) to a unit of medication. The element contains the numerator and denominator of the strength ratio.

The IDMP ISO 11238 standard addresses the identification and exchange of regulated information on substances.  The Global Ingredient Archival System (GInAS.html)  will provide a common global identifier for all of the substances used in medicinal products, providing a definition of substances globally consistent with this standard. Those identifiers however are yet available for concrete usage, therefore in this version of the template, SNOMED CT has been chosen as reference terminology also for the active substances. This choice will be revised based on the availability and the maturity of GInAS.

This element can be used to provide alternative identifications for the described substance.

Name of the substance

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This element is generally used to identify a medicinal product. When the IDMP identifiers will be concretely available for usage this element will be used for conveying the Medicinal Product Identifier (MPID.html). For the time being, it could be optionally used for conveying jurisdictional or agreed cross jurisdictional medicinal product code.

This element is supposed to be valorized with the complete Medicinal Product Name as approved by the Medicines Regulatory Agency in a jurisdiction.

The name may be applicable in one or more country/language combinations.

When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

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When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

A unique identifier that guarantees the global uniqueness of the instance identifier. The root alone may be the entire instance identifier.

When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

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When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

A unique identifier that guarantees the global uniqueness of the instance identifier. The root alone may be the entire instance identifier.

This element is generally used to identify a medicinal product. When the IDMP identifiers will be concretely available for usage this element will be used for conveying the Medicinal Product Identifier (MPID.html). For the time being, it could be optionally used for conveying jurisdictional or agreed cross jurisdictional medicinal product code.

This element is supposed to be valorized with the complete Medicinal Product Name as approved by the Medicines Regulatory Agency in a jurisdiction.

The name may be applicable in one or more country/language combinations.

Base definition for all types defined in FHIR type system.

When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

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When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

If a value is an exceptional value (NULL-value), this specifies in what way and why proper information is missing.

A human readable name or mnemonic for the assigning authority. The Assigning Authority Name has no computational value. The purpose of a Assigning Authority Name is to assist an unaided human interpreter of an II value to interpret the authority. Note: no automated processing must depend on the assigning authority name to be present in any form.

Specifies if the identifier is intended for human display and data entry (displayable = true) as opposed to pure machine interoperation (displayable = false).

A unique identifier that guarantees the global uniqueness of the instance identifier. The root alone may be the entire instance identifier.

A character string as a unique identifier within the scope of the identifier root.

If a value is an exceptional value (NULL-value), this specifies in what way and why proper information is missing.

When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

• value @ root
• value @ root,

When valued in an instance, this attribute signals the imposition of a set of template-defined constraints. The value of this attribute provides a unique identifier for the templates in question

If a value is an exceptional value (NULL-value), this specifies in what way and why proper information is missing.

A human readable name or mnemonic for the assigning authority. The Assigning Authority Name has no computational value. The purpose of a Assigning Authority Name is to assist an unaided human interpreter of an II value to interpret the authority. Note: no automated processing must depend on the assigning authority name to be present in any form.

Specifies if the identifier is intended for human display and data entry (displayable = true) as opposed to pure machine interoperation (displayable = false).

A unique identifier that guarantees the global uniqueness of the instance identifier. The root alone may be the entire instance identifier.

A character string as a unique identifier within the scope of the identifier root.

This element is generally used to identify a medicinal product. When the IDMP identifiers will be concretely available for usage this element will be used for conveying the Medicinal Product Identifier (MPID.html). For the time being, it could be optionally used for conveying jurisdictional or agreed cross jurisdictional medicinal product code.

This element is supposed to be valorized with the complete Medicinal Product Name as approved by the Medicines Regulatory Agency in a jurisdiction.

The name may be applicable in one or more country/language combinations.