Food safety and quality

Publications

Search for a publication

Free Text
This volume of FAO JECFA Monographs contains specifications of identity and purity prepared at the 84th meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), held in Rome, Italy, 6–15 June 2017 . The specifications monographs are one of the outputs of JECFA’s risk assessment of food additives, and should be read in conjunction with the safety evaluation, reference to which is made in the section at the head of each specifications monograph. Further information on the meeting discussions can be found in the summary report of the meeting and in the full report which will be published in the WHO Technical Report series. Toxicological monographs of the substances considered at the meeting will be published in the...
2017
These FAO guidance materials were developed to support food safety risk managers and policy-makers in applying structured, evidence-informed processes to decisionmaking. Food safety issues can have widespread impacts beyond public health. They may contribute to, or detract from the achievement of goals in areas including nutrition, food security, food trade and market access, economic and rural development. The risk analysis paradigm guides risk managers to ensure their decisions are based on an assessment of risks to health, and consideration of other factors in choosing the preferred risk management decision. The materials assist decision-makers in applying a multi-factor approach and is applied to two key decision areas – setting food safety priorities, and selecting risk management options. The principles and approaches...
2017
This volume of FAO JECFA Monographs contains residue evaluation of certain veterinary drugs prepared at the 81st Meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), held in Rome, Italy, 17–26 November 2015. This JECFA meeting was convened specifically to consider residues of veterinary drugs in food-producing animal species, to further elaborate principles for evaluating the safety of residues of veterinary drugs in food and for establishing acceptable daily intakes (ADIs) a nd/or acute reference doses (ARfDs), and to recommend maximum residue limits (MRLs) for substances on the agenda when they are administered to food-producing animals in accordance with good veterinary practice in the use of veterinary drugs. The monographs contained therein provide the scientific basis for the...
2016