Quality: non-immunologicals

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The European Medicines Agency’s scientific guidelines on the non-immunologicals help medicine developers prepare marketing authorisation applications for veterinary medicines.

If you have comments on a document which is open for consultation, use the form for submission of comments on scientific guidelines.

For a complete list of scientific guidelines currently open for consultation, see Public consultations.


Development pharmaceuticals

Guidelines

 
Manufacture of medicinal product

Guidelines


Active substance

Guidelines


Reflection papers


Documents of interest


Impurities

Guidelines


Excipients

Guidelines


Reflection papers


Packaging

Guidelines



Specifications, analytical procedures and analytical validation

Guidelines


Reflection papers


Transmissible spongiform encephalopathies (TSEs)

Guidelines


Stability

Guidelines


Herbal medicinal products

Guidelines


Specific veterinary dosage forms

Guidelines


Position papers

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