Medicines (Oral Dental Gums) (Licensing) Regulations

Medicines Act

(Chapter 176, Sections 14, 54 and 74)

Rg 18

G.N. No. S 660/2003

REVISED EDITION 2005

(31st March 2005)

[1st January 2004]

Citation

1. These Regulations may be cited as the Medicines (Oral Dental Gums) (Licensing) Regulations.

Definition

2. In these Regulations, unless the context otherwise requires, “oral dental gum” shall have the same meaning as in the Medicines (Oral Dental Gums) (Specification) Order (O 19).

Standard provisions for licences

3. The standard provisions for licences to be granted under Part II of the Act in respect of oral dental gum shall be as follows:

(a)	for a product licence, the provisions set out in the First Schedule;
(b)	for an import licence, the provisions set out in the Second Schedule;
(c)	for a wholesale dealer’s licence, the provisions set out in the Third Schedule; and
(d)	for a manufacturer’s licence, the provisions set out in the Fourth Schedule.

Duration of licence

4. A licence granted under Part II of the Act in respect of oral dental gum shall be valid for a period of one year or such other duration as the licensing authority may determine.

Fees

5.—(1) The fees specified in the Fifth Schedule shall be payable to the licensing authority on application for, or the grant of, licences in respect of oral dental gum and for any variation of the licences.

(2) No refund shall be made in respect of any fee paid under these Regulations.

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