Quality: non-immunologicals

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 Microsoft Office document iconform 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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