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§1301.20. Registration for emergency medical services agencies. — Inbound Citations

21 C.F.R. § 1301.20

Cited by 3 regulations in release Current.

Citations to 21 C.F.R. § 1301.20 as a whole

  • (2) A designated location of the agency 30 days following notification to DEA in accordance with § 1301.20;
  • (a) Each emergency medical services agency registered pursuant to § 1301.20 of this chapter (including a hospital-based emergency medical services agency using a hospital registration under § 1301.20(a)(2) of this chapter) must maintain records for each dose of controlled substances administered or disposed of in the course of providing emergency medical services. The following information shall be included in each record:
    (1) Name of the substance;
    (2) Finished form of the substance (e.g., 10-milligram tablet or 10-milligram concentration per fluid ounce or milliliter);
    (3) Date administered or disposed of;
    (4) Identification of the patient (consumer), if applicable;
    (5) Amount administered;
    (6) Last name or initials of the person who administered the controlled substance;
    (7) Last name or initials of the medical director or authorizing medical professional issuing the standing or verbal order;
    (8) Whether a standing or verbal order was issued and adopted;
    (9) Amount disposed of, if applicable;
    (10) Manner disposed of; and

Citations to §1301.20(a)(2)

  • (a) Each emergency medical services agency registered pursuant to § 1301.20 of this chapter (including a hospital-based emergency medical services agency using a hospital registration under § 1301.20(a)(2) of this chapter) must maintain records for each dose of controlled substances administered or disposed of in the course of providing emergency medical services. The following information shall be included in each record:
    (1) Name of the substance;
    (2) Finished form of the substance (e.g., 10-milligram tablet or 10-milligram concentration per fluid ounce or milliliter);
    (3) Date administered or disposed of;
    (4) Identification of the patient (consumer), if applicable;
    (5) Amount administered;
    (6) Last name or initials of the person who administered the controlled substance;
    (7) Last name or initials of the medical director or authorizing medical professional issuing the standing or verbal order;
    (8) Whether a standing or verbal order was issued and adopted;
    (9) Amount disposed of, if applicable;
    (10) Manner disposed of; and