• Draft Guideline Released by EMA on Pharmacological ADIs for Veterinary Medicinal Products

    The European Medicines Agency (EMA)  released a draft guideline  on 23 January on pharmacological acceptable daily intake (ADI), titled Guideline on the approach to establish a pharmacological ADI . The guideline advises when to establish a pharmacological ADI, how to conduct studies and what endpoints must be addressed. EU legislation requires that any food produced from animals that are treated with veterinary medicinal products be free from medicinal residu...