European Commission: Contribution submitted in response to the Public Consultation Paper on a Contribution for a future Commission regulation on the format and content for applications and requests for an opinion on a maximum residue limit for a pharmacol

From 11 May 2009 till 6 July 2009 the Directorate General for Enterprise and Industry invited stakeholders to comment on a contribution to the preparation of a future Commission regulation on the format and content for applications and requests for an opinion on a maximum residue limit for a pharmacologically active substance prepared by the European Medicines Agency and its Committee for Veterinary Medicinal Products (\'CVMP\'). In response to this consultation, IFAH-Europe sent in comments on the contribution.