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POME RM010100
Revision as of 20:40, 19 May 2011 by Rob hallowell (talk | contribs)
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This page documents Known issues, Change Requests, Planned Changes and Actual Change History for the RMIM or DMIM specified. Changes between current and previously balloted versions are held on the actual visio.
The latest version of the visio that is held on subversion is accessible here
Known issues
ID | Started by | Description |
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1 | N Ewon | xxxxxxxxxxxxxxxxx |
Change Requests
ID | Started by | Description |
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1 | N Ewon | xxxxxxxxxxxxxxxxx |
Planned Changes
ID | Started by | Description |
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======= | ======================= | ====================================== |
1 | N Ewon | xxxxxxxxxxxxxxxxx |
Change History
v 1.3.0 - 10 Mar 2006
- ManufacturedMaterial2.code: changed x_Medicine,
- Loosened cardinalities
- Removed MaxLen constraints
- Renamed acts to match DMIM i.e:
- ManufacturedMaterial To Medicine
- ManufacturedMaterialKind to Ingredient
- ManufacturedMaterial2 to MedicineClass
- ContainerKind toPackagedMedicine
- DrugChraracteristicEvent to Characteristic
v 1.3.2 - 25 Jul 2006
- Removed DrugStrengthDescriptionObservationEvent3
- Removed all Canadian-link for sorting: A, B, …
v1.4.1 - 1 March 2008
- Changed RoleClassCode of Medication from MED to ADMM
- Changed Characteristic.code to use MedicationObservationType in place of FDALabelData
- Replaced FinancialTransactionDefinition with A_Pricing CMET
- Relaxed vocabulary for PackagedMedicine.code form CompliancePackageEntityType to ContainerEntityType
- Relaxed vocabulary for PackagedMedicine.code from MedicationCap to ContainerCap
- Corrrected data type for Content.quantity from PQ to RTO
v1.4.2 - 04 March 2008
- Corrected artifact ID for A_Pricing CMET
v1.5.0 - 15 November 2010
- Added Acts for Route and Indication
- Added Entity for Manufacturer Name