Did registrants have a say in any of the changes to AIMS?

A 60-day open consultation was held to gather feedback on the proposed changes to the AIMS supplemental Standard of Practice prior to approval at the December 2025 Board meeting. The Board decision to allow pharmacies autonomy to select their own medication incident reporting platform (provided it meets requirements and contributes to NIDR) as well as assigning responsibility for costs did not require consultation; however, information on this decision was included in the consultation materials posted.