Pharmaceutical Quality (Industry)
1.0.0 - STU1 International flag

Pharmaceutical Quality (Industry), published by HL7 International / Biomedical Research and Regulation. This guide is not an authorized publication; it is the continuous build for version 1.0.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/HL7/uv-dx-pq/ and changes regularly. See the Directory of published versions

ValueSet: Impurity Types

Official URL: http://hl7.org/fhir/uv/pharm-quality/ValueSet/vs-impurity-type-pq Version: 1.0.0
Active as of 2024-05-08 Computable Name: VsImpurityTypePQ
Other Identifiers: OID:2.16.840.1.113883.4.642.40.41.48.14

This value set contains codes for impurity type.

References

Logical Definition (CLD)

 

Expansion

Expansion based on codesystem Impurity Type Codes v1.0.0 (CodeSystem)

This value set contains 4 concepts.

CodeSystemDisplay
  CH-IMPhttp://terminology.hl7.org/CodeSystem/impurity-typeChiral Impurity
  INT-IMPhttp://terminology.hl7.org/CodeSystem/impurity-typeProcess intermediate, forced degradation product
  PR-IMPhttp://terminology.hl7.org/CodeSystem/impurity-typeProcess impurity
  ST-IMPhttp://terminology.hl7.org/CodeSystem/impurity-typeStarting material, forced degradation product

Explanation of the columns that may appear on this page:

Level A few code lists that FHIR defines are hierarchical - each code is assigned a level. In this scheme, some codes are under other codes, and imply that the code they are under also applies
System The source of the definition of the code (when the value set draws in codes defined elsewhere)
Code The code (used as the code in the resource instance)
Display The display (used in the display element of a Coding). If there is no display, implementers should not simply display the code, but map the concept into their application
Definition An explanation of the meaning of the concept
Comments Additional notes about how to use the code