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
Basic information
Dates Date of document:
  • March 10, 1995
Date of publication:
  • March 11, 1995
Date of effect:
  • March 14, 1995
    • Entry into force - Date pub. + 3 See Art 5
Modified by
Modifies
Affected by case
Legal basis
EuroVoc Vocabulary
  • Medicinal product
  • Public health
  • Consumer information
  • Consumer protection
  • Market approval
  • Health risk
  • Proprietary medicinal products
  • Trade information