203.30—Sample distribution by mail or common carrier.
(a) Requirements for drug sample distribution by mail or common carrier.
A manufacturer or authorized distributor of record may distribute a drug sample to a practitioner licensed to prescribe the drug that is to be sampled or, at the written request of a licensed practitioner, to the pharmacy of a hospital or other health care entity, by mail or common carrier, provided that:
(1)
The licensed practitioner executes and submits a written request to the manufacturer or authorized distributor of record, as set forth in paragraph (b) of this section, before the delivery of the drug sample;
(2)
The manufacturer or authorized distributor of record verifies with the appropriate State authority that the practitioner requesting the drug sample is licensed or authorized under State law to prescribe the drug product;
(3)
The recipient executes a written receipt, as set forth in paragraph (c) of this section, when the drug sample is delivered; and
(4)
The receipt is returned to the manufacturer or distributor from which the drug sample was received.
(b) Contents of the written request form for delivery of samples by mail or common carrier.
(1)
A written request for a drug sample to be delivered by mail or common carrier to a licensed practitioner is required to contain the following:
(ii)
The practitioner's State license or authorization number or, where a scheduled drug product is requested, the practitioner's Drug Enforcement Administration number.
(v)
The name of the manufacturer and the authorized distributor of record, if the drug sample is requested from an authorized distributor of record; and
(2)
A written request for a drug sample to be delivered by mail or common carrier to the pharmacy of a hospital or other health care entity is required to contain, in addition to all of the information in paragraph (b)(l) of this section, the name and address of the pharmacy of the hospital or other health care entity to which the drug sample is to be delivered.
(c) Contents of the receipt to be completed upon delivery of a drug sample.
The receipt is to be on a form designated by the manufacturer or distributor, and is required to contain the following:
(1)
If the drug sample is delivered to the licensed practitioner who requested it, the receipt is required to contain the name, address, professional title, and signature of the practitioner or the practitioner's designee who acknowledges delivery of the drug sample; the proprietary or established name and strength of the drug sample and the quantity of the drug sample delivered; and the date of the delivery.
(2)
If the drug sample is delivered to the pharmacy of a hospital or other health care entity at the request of a licensed practitioner, the receipt is required to contain the name and address of the requesting licensed practitioner; the name and address of the hospital or health care entity pharmacy designated to receive the drug sample; the name, address, professional title, and signature of the person acknowledging delivery of the drug sample; the proprietary or established name and strength of the drug sample; the quantity of the drug sample delivered; and the date of the delivery.