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AVMA policy
 
Adverse Event Reporting
(Oversight: COBTA: EB approved 03/06; reaffirmed 04/11)
 

Being committed to the continuing availability of medicinal products that are pure, safe, potent and efficacious for animals, the AVMA encourages continued development and strengthening of adverse event reporting systems. This includes continued collaboration with constituent professional organizations, industry organizations, government entities and other stakeholders.

See also: Reporting adverse events