Toxicological Evaluation of Certain Veterinary Drug Residues in Food
Seventy-eighth Meeting of the Joint FAO/WHO Expert Committee on Food Additives
- Publisher
World Health Organization - Published
20th February 2015 - ISBN 9789241660693
- Language English
- Pages 246 pp.
- Size 8.25" x 11.75"
- Images tables
This volume contains monographs prepared at the seventy-eighth meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), which met in Geneva, Switzerland, from 5 to 14 November 2013.
The toxicological monographs in this volume summarize data on the veterinary drug residues that were evaluated toxicologically by the Committee: gentian violet, lasalocid sodium, recombinant bovine somatotropins and zilpaterol hydrochloride. Annexed to the report is a summary of the Committee's recommendations on these and other drugs discussed at the seventy-eighth meeting, including acceptable daily intakes (ADIs) and proposed maximum residue limits (MRLs).
This volume and others in the WHO Food Additives Series contain information that is useful to those who produce and use food additives and veterinary drugs and those involved with controlling contaminants in food, government and food regulatory officers, industrial testing laboratories, toxicological laboratories and universities.
World Health Organization
World Health Organization is a Specialized Agency of the United Nations, charged to act as the world's directing and coordinating authority on questions of human health. It is responsible for providing leadership on global health matters, shaping the health research agenda, setting norms and standards, articulating evidence-based policy options, providing technical support to countries, and monitoring and assessing health trends.