FDA Releases Revised Guidance on Safety of Veterinary Drug Residues in Human Food

Summary

The Food and Drug Administration (FDA) has made available a revised guidance document, VICH GL36(R), which provides a general approach to establishing a Microbiological Acceptable Daily Intake (ADI) for residues of veterinary antimicrobial drugs in human food, developed by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH).