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Pharmacovigilance - will human pharmaceuticals affect the veterinary side?

European regulators are starting to focus more on pharmacovigilance data to evaluate a medicine's safety and efficacy in the EU, following the introduction of the new EU medicines legislation, which puts greater emphasis on the risk/ benefit balance. However, regulators in the human pharmaceutical industry have conceded that regulation on pharmacovigilance is too "complex". Sita Shah explores whether this will prompt changes on the veterinary side.


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