Safety and residue data requirements for veterinary medicinal products intended for minor use or minor species (MUMS)/limited market

Current version

PDF iconAdopted guideline - Revision 1

Currently under revision - see below

Reference numberEMA/CVMP/SWP/66781/2005 Rev. 1
Published03/01/2017
Effective from01/07/2017
KeywordsMinor uses/minor species (MUMS), data requirements
DescriptionThis 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

PDF iconDraft guideline - Revision 2 ​​​

 

 

PDF iconConcept paper

Published: 18/12/2018

Deadline for comments: 31/08/2019

 

Published: 26/01/2018

Deadline for comments: 28/02/2018

Revision 1
Current version

 

Adopted guideline

 

PDF iconOverview of comments

 

PDF iconDraft guideline - Revision 1

Published: 03/01/2017
Effective from: 01/07/2017

 

Published: 03/01/2017

 

Published: 03/02/2016

First version

PDF iconAdopted guideline

 

PDF iconOverview of comments

In operation: 01/02/2007-present

 

Published: 20/07/2006

Superseded document PDF iconAdopted guideline In operation: 12/11/1997-01/02/2007

 

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