# The Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994, Paragraph 5


A manufacturing and control file for each pharmaceutical form and a description of the method of dilution and potentization.

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Source: https://www.legislation.gov.uk/uksi/1994/105/schedule/1/paragraph/5 (the official version)
Page: https://openlegislation.uk/medicines-homoeopathic-medicinal-products-for-human-use-regulations-1994/schedule-1/paragraph-5
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.