Singapore legislation

Regulation 37

of Health Products (Therapeutic Products) Regulations 2016

Regulation 37

Duty of licensed importer

Without prejudice to any other provision in this Part, a holder of an importer’s licence for a therapeutic product —

(a)

must ensure, and maintain objective evidence to establish, that the handling and storage of the therapeutic product complies with any standard set out by the Authority on the Authority’s website for the therapeutic product;

(b)

must provide and maintain, or ensure the provision and maintenance of, such staff, premises, equipment and facilities for the handling and storage of the therapeutic product as are necessary to prevent the deterioration of the therapeutic product while it is in the holder’s ownership, possession or control; and

(c)

must not use, for any purpose mentioned in paragraph (b), any premises other than the premises specified in the holder’s licence, or such other premises as may be approved from time to time by the Authority.