This set of Vetinnova includes a series of requirements that are required during the presentation of the documentation of a record of veterinary drugs, both pharmacological and immunological. These requirements do not imply an exhaustive list of all the existing ones, but a compilation of those that have been considered relevant, organizing in an easy and intuitive way for the research group.
Although Vet + i will periodically update the contents of this section, it is recommended to check the validity of these documents through the web pages of the different international, European and national institutions responsible for their edition. In addition, the National Regulatory Authority can be consulted (AEMPS)
Below is a series of links to the institutions where you can find information on the regulatory requirements in this field:
|Quality guidelines:||Safety and residues guidelines:|
|Non-immunologicals||Availability (minor uses / minor species)|
|Availability (minor uses minor species)||Multidisciplinary|
|Multidisciplinary||Biocides for use in animal husbandry|
|Efficacy guidelines:||Immunological guidelines:|
|Availability (minor uses / minor species)||Stability|
|Multidisciplinary||Availability (minor uses / minor species)|
Eudralex - Normativa sobre medicamentos en la Unión Europea:
III.- State scope Organizations:
AEMPS- Agencia Española de Medicamentos y Productos Sanitarios. Medicamentos veterinarios.
Investigación clínica con medicamentos veterinarios.
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