Why is manufacturing information limited to a single Organization reference?

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    • Type: Change Request
    • Resolution: Unresolved
    • FHIR Core (FHIR)
    • R4
    • Biomedical Research & Regulation
    • MedicinalProductDefinition
      PackagedProductDefinition
    • Enhancement

      Doesn't the regulatory process need more information - such as authorized sites, who's responsible for different manufacturing stages, etc?

      Proposed Wording:

      lloyd@lmckenzie.com

      (Comment 28 - imported by: Ron G. Parker)

            Assignee:
            Unassigned
            Reporter:
            Ron Parker
            Lloyd McKenzie, Ron Parker
            Watchers:
            3 Start watching this issue

              Created:
              Updated: