(1)  This regulation applies to –

(a) a person engaged in the manufacture of, or wholesale dealing in, any substance specified in Schedule 1 or 4 to the Poisons List; and

(b) the agent of any such person –

who lawfully supplies any of those substances by way of free distribution as a clinical sample.

(2)  Any person to whom this regulation applies must, on each occasion upon which the person supplies any substance referred to in subregulation (1) by way of free distribution, make a record of the supply showing –

(a) the date of the supply; and

(b) the name and address of the person to whom the substance was supplied; and

(c) the name and quantity of the substance so supplied.

(3)  Except in the case of the supply of the substance referred to in subregulation (1) by registered or certified mail, a person supplying the substance must obtain a receipt at the time of supply from the person to whom the supply was made.

(4)  The provisions of regulation 77(2) and (3) apply, with any necessary modification, to the records and receipts required to be made under this regulation.