# Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance), Division (d): Stability tests

Extent: E+W+S+N.I.

The stability of the finished product shall be demonstrated. Stability data from the homeopathic stocks are generally transferable to dilutions/potentisations obtained thereof. If no identification or assay of the active substance is possible due to the degree of dilution, stability data of the pharmaceutical form may be considered.

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Source: https://www.legislation.gov.uk/eur/2019/6/annex/II/title/IV/division/2/part/2/division/d (the official version)
Page: https://openlegislation.uk/eu-regulation-2019-6/annex-II/title-IV/division-2/part-2/division-d
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.