Oregon Administrative Rules
Chapter 332 - OREGON HEALTH AUTHORITY, HEALTH LICENSING OFFICE, BOARD OF DIRECT ENTRY MIDWIFERY
Division 26 - LEGEND DRUGS AND DEVICES
Section 332-026-0000 - Access to and Administration of Legend Drugs and Devices

(1) An LDM is prohibited from purchasing or administering legend drugs and devices, until the continuing education listed in OAR 332-020-0010 has been completed and attestation submitted to the Office upon renewal.

(2) Pursuant to ORS 687.493, an LDM who completes the continuing education listed in OAR 332-020-0010 is authorized to purchase and administer legend drugs and devices listed in OAR 332-026-0010, 332-026-0020, and 332-026-0030.

(3) An LDM must comply with all local, state and federal laws and regulations regarding the administration, distribution, storage, transportation and disposal of legend drugs and devices listed in OAR 332-026-0010, 332-026-0020, 332-026-0030.

(4) Approved legend drugs must be inventoried and securely stored when the product is not in use, including samples or any remaining portion of a drug.

(5) Records regarding approved legend drugs and devices must be maintained for five years. Records must be kept on the business premises and available for inspection upon request by the Office. Upon request by the Board or Office an LDM must provide a copy of records. Records must include, but are not limited, to the following:

(6) Expired, deteriorated or unused legend drugs must be disposed of in a manner that protects the LDM, client and others who may come into contact with the material during disposal.

(7) An LDM is required to obtain education and training before administering or purchasing any legend drug or device.

(8) An LDM is not required to administer and purchase any legend drugs or devices.