# The Veterinary Medicines Regulations 2007, Paragraph 15: Similar immunological products


Where an immunological veterinary medicinal product is pharmacologically equivalent to a reference product other than differences in raw materials or in the manufacturing process, the results of the appropriate pre-clinical tests or clinical trials must be provided, but the applicant need not provide the results of safety tests or residue tests.

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Source: https://www.legislation.gov.uk/uksi/2007/2539/schedule/1/paragraph/15 (the official version)
Page: https://openlegislation.uk/veterinary-medicines-regulations-2007/schedule-1/paragraph-15
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.