Federal Register #C1-2026-02288

DEA Rule: Registration Requirements for EMS Agencies Accessing Emergency Medications

The Drug Enforcement Administration (DEA), part of the Department of Justice, has issued a rule establishing registration requirements for Emergency Medical Services (EMS) agencies under the Protecting Patient Access to Emergency Medications Act of 2017. - Government Buyer: - Department of Justice - Drug Enforcement Administration (DEA) - OEMs and Vendors: - DEA is the only entity mentioned; no commercial OEMs or vendors are involved - Products/Services Requested: - No products, part numbers, or purchase quantities are specified - This is a regulatory rule, not a procurement for goods or services - Unique or Notable Requirements: - Establishes registration, compliance, and enforcement provisions for EMS agencies seeking access to emergency medications - Aims to ensure proper access to emergency medications while maintaining regulatory oversight - No additional unique requirements beyond registration and compliance provisions - Period of Performance: - Rule is effective upon publication

Description

This rule establishes the registration requirements for Emergency Medical Services (EMS) agencies under the Protecting Patient Access to Emergency Medications Act of 2017. It outlines regulatory provisions related to the registration process, compliance, and enforcement as administered by the Drug Enforcement Administration. The rule is effective upon publication and aims to ensure EMS agencies have proper access to emergency medications while maintaining regulatory oversight.

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