Medicines (Good Manufacturing Practice Certificate) Regulations 2002

Status:

Published in Subsidiary Legislation Supplement
on 22 Mar 2002

No. S 130

Medicines Act

(Chapter 176)

Medicines (Good Manufacturing Practice Certificate) Regulations 2002

In exercise of the powers conferred by section 74 of the Medicines Act, the Minister for Health hereby makes the following Regulations:

Citation and commencement

1. These Regulations may be cited as the Medicines (Good Manufacturing Practice Certificate) Regulations 2002 and shall come into operation on 1st June 2002.

Definitions

2. In these Regulations, unless the context otherwise requires —

“active pharmaceutical ingredient” means any raw material which is used as an active ingredient in the manufacture of a medicinal product;

“Good Manufacturing Practice Certificate” or “GMP Certificate” means a certificate relating to the manufacture of any medicinal product or active pharmaceutical ingredient attesting to its conformity with a Good Manufacturing Practice Standard;

“Good Manufacturing Practice Standard” means the Pharmaceutical Inspection Convention/Pharmaceutical Inspection Co-Operation Scheme Guide to Good Manufacturing Practice for medicinal products or active pharmaceutical ingredients (as the case may be) or such other good manufacturing practice standard approved by the licensing authority.

Application for GMP Certificate

3.—(1) For the purposes of section 22 of the Act, an application for a GMP Certificate shall be made to the licensing authority in such form and manner as the licensing authority may require.

(2) Upon receipt of an application under paragraph (1), the licensing authority may, upon assessment of satisfactory conformity with a Good Manufacturing Practice Standard, issue a GMP Certificate to the manufacturer of any medicinal product or active pharmaceutical ingredient, subject to such terms and conditions as the licensing authority thinks fit.

(3) Every GMP Certificate issued under paragraph (2) shall be valid for a period not exceeding 2 years from the date of the certificate.

Fees

4.—(1) The fees payable for a GMP Certificate shall be as follows:

(a)	on application for a GMP Certificate

—

$4,000; and

(b)	for each additional GMP Certificate which does not require further assessment of conformity with any Good Manufacturing Practice Standard

—

$200.

(2) No refund shall be made in respect of any fee paid under paragraph (1).

Made this 13th day of March 2002.

MOSES LEE

Permanent Secretary,
Ministry of Health,
Singapore.

[CPA(MQA)78:01/2; AG/LEG/SL/176/2002/1 Vol. 1]

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