Since July 1, 2026, Indiana law has excused some drug reports, required consent for opioid treatment program reports, and allowed limited sharing of monitoring data.
Dispensers do not have to report a drug given directly to a patient or a veterinarian’s supply of certain controlled drugs lasting no more than 72 hours.
Before reporting patient information to INSPECT, an opioid treatment program must get the patient’s consent under federal rules.
The board may share prescription monitoring data with certain state agency representatives to help with an active controlled substance investigation or prevent overdoses.
Dispensers do not have to send certain drug information to INSPECT. This applies to information dispensers otherwise must report under the INSPECT rules. The exception covers a drug given directly to a patient or a veterinary practitioner’s supply of no more than 72 hours of a Schedule II, III, IV, or V controlled drug. These provisions took effect July 1, 2026.
Opioid treatment programs must get patient consent before reporting patient information to INSPECT. The requirement applies when an opioid treatment program reports patient information to INSPECT. Programs must follow the consent rules in federal regulations 42 CFR 2.36 and 42 CFR 2.31. This provision took effect July 1, 2026.
The board may share prescription monitoring data with certain state agency representatives. The recipients may be representatives of the Indiana Department of Health or the office of the secretary of family and social services. The data may be shared to aid an active investigation concerning a controlled substance or help prevent overdose events. This provision took effect July 1, 2026.
No hearings or votes scheduled.