Reporting Chemical ‘Non-Performances’ or ‘Adverse Experiences’

The Adverse Experience Reporting Program (AERP) is a post-registration program that assesses reports of adverse experiences associated with the use of a registered chemical product (or those on minor use permit). Reporting must now be completed ONLINE. Reports of adverse experiences are closely monitored by the APVMA and it is vital to record, assess and classify adverse experiences to detect uncommon events not evident during the initial registration process of a product.