Draft report on the development of a harmonised approach to exposure assessment methodologies for residues from veterinary medicinal products, feed additives and pesticides in food of animal origin

July 5, 2022

In 2020, the European Commission (EC) requested EMA and European Food Safety Authority (EFSA) for advice for the development of a harmonised approach on exposure assessment methodologies for residues from veterinary medicinal products (EMA), feed additives and pesticides in food of animal origin (EFSA). This work was undertaken under the EC mandate by a working group composed of CVMP experts, EFSA experts, specialists with expertise from the Joint FAO / WHO Expert Committee on Food Additives (JECFA) and the Joint Meeting on Pesticide Residues (JMPR), and an European Chemichal Agency (ECHA) observer. The draft report compares available models of consumer exposure and makes recommendation on a harmonised approach to be used by EMA and EFSA for the assessment of exposure to residues of veterinary medicines, feed additives and pesticides in food of animal origin.

Download the Draft Report

Interested in learning more? Contact us today to find out how we can help with your global regulatory needs




EMA EU

July 5, 2022

Products Management Services - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe Introduction - EU Implemen

The Europe Introduction - EU Implementation Guide has been prepared by the European Medicines Agency (EMA) upon consultation with different stakeholders (representatives of marketing authorisation...

Read More

July 5, 2022

Meet the Expert: Lucy Radley

Our “Meet the Expert” series introduces you to our team of experts around the world. This “behind the curtain” view will help you get to know who we are on a professional and personal level, and...

Read More
EMA Europe

July 5, 2022

Advice on the designation of antimicrobials or groups of antimicrobials reserved for treatment of certain infections in humans - in relation to implementing measures under Article 37(5) of Regulation

Regulatory and Procedural Guideline May 2022 EMA/CVMP/678496/2021-rev Introduction “According to Article 37(5) of Regulation (EU) 2019/6 (‘the Regulation’), the European Commission shall adopt...

Read More