# Commission Regulation (EC) No 540/95 of 10 March 1995 laying down the arrangements for reporting suspected unexpected adverse reactions which are not serious, whether arising in the Community or in a third country, to medicinal products for human or veterinary use authorized in accordance with the provisions of Council Regulation (EEC) No 2309/93

EU Regulation No 540/1995 · adopted 10 March 1995

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Source: https://www.legislation.gov.uk/eur/1995/540 (the official version)
Page: https://openlegislation.uk/eu-regulation-1995-540
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.