Safety and residue data requirements for veterinary medicinal products intended for minor use or minor species (MUMS)/limited market
| Current version |
Currently under revision - see below |
| Reference number | EMA/CVMP/SWP/66781/2005 Rev. 1 |
| Published | 03/01/2017 |
| Effective from | 01/07/2017 |
| Keywords | Minor uses/minor species (MUMS), data requirements |
| Description | This document defines the acceptable data requirements for safety and residues documentation for veterinary medicinal products intended for minor uses or minor species. |
Document history
| Revision 2 |
|
Published: 18/12/2018 Deadline for comments: 31/08/2019
Published: 26/01/2018 Deadline for comments: 28/02/2018 |
|
Revision 1
|
|
Published: 03/01/2017
Published: 03/01/2017
Published: 03/02/2016 |
| First version |
In operation: 01/02/2007-present Published: 20/07/2006 |
|
| Superseded document |
 Adopted guideline
|
In operation: 12/11/1997-01/02/2007 |
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Concept paper for the revision of the guidelines on data 4 requirements for veterinary medicinal products for minor use minor species (EMEA/CVMP/IWP/123243/2006-Rev.2), (EMEA/CVMP/QWP/128710/2004),(EMEA/CVMP/SWP/66781/2005),(EMEA/CVMP/EWP/117899/2004)
- Directive 2001/82/EC
- Directive 2009/9/EC
- Regulation (EC) No 470/2009
- Commission Regulation 2018/782