1. The holder of a manufacturing authorisation shall record the following information in respect of all veterinary medicinal products that it supplies:
(a)
date of the transaction;
(b)
name of the veterinary medicinal product, and marketing authorisation number if applicable, as well as pharmaceutical form and strength, as appropriate;
(c)
quantity supplied;
(d)
name or company name and permanent address or registered place of business of the recipient;
(e)
batch number;
(f)
date of expiry.
2. The records referred to in paragraph 1 shall be available for inspection by competent authorities for one year after the date of expiry of the batch or at least five years from recording, whichever is longer.