A 26
[Subsidiary]
L.N. 137/78.
L.N. 137/78.
CAP. 138]
Pharmacy and Poisons Regulations
[1987 Ed.
by or under the law of the country in which they are or are to be manufactured have been or will be complied with.
(4) The Committee shall make arrangements for the separate processing of an application for the registration of a new pharmaceutical product or new substance so that its registration shall not be unduly delayed.
(5) For the purposes of paragraph (4) “new pharmaceutical product” and “new substance” means a medicine containing an active ingredient, or a substance, having a chemical formula which has not previously been marketed or registered in Hong Kong under some other name or description.
L.N. 369/80.
Application for
registration
under section
28A.
Eighth Schedule,
Form 13.
Ninth Schedule.
Eighth Schedule, Form 14.
PART VIIIA
REGISTRATION OF IMPORTERS AND EXPORTERS
37A. (1) Any application for registration under section 28A as an importer or exporter of pharmaceutical products shall be made to the Committee in Form 13 in the Eighth Schedule and shall be accompanied by the fee specified in the Ninth Schedule.
(2) The Committee may require any applicant under this regulation to furnish such information and to permit such inspection of premises and storage facilities used by the applicant for the purposes of his business as the Committee may specify by notice to the applicant.
(3) The Committee may grant or refuse any application under this regulation as the Committee may deem fit.
(4) The Committee shall furnish any person whose application is granted with a certificate in Form 14 in the Eighth Schedule.
(5) Any person aggrieved by a decision of the Committee under this regulation may, in the prescribed manner, appeal to the Tribunal against that decision.
Disclosure of composition of medicines. L.N. 137/78.
PART IX
SALE OF MEDICINES
38. (1) Subject to these regulations, no person shall—
(a) sell any article consisting of or comprising a substance recommended as a medicine; or
(b) supply any such article as a sample for the purpose of inducing persons to buy the substances of which it consists or which it comprises,
unless—
(i) the article is labelled as required under regulation 31; or
A 26
[Subsidiary]
L.N. 137/78.
L.N. 137/78.
CAP. 138]
Pharmacy and Poisons Regulations
[1987 Ed.
by or under the law of the country in which they are or are to be manufactured have been or will be complied with.
(4) The Committee shall make arrangements for the separate processing of an application for the registration of a new phar- maceutical product or new substance so that its registration shall not be unduly delayed.
(5) For the purposes of paragraph (4) “new pharmaceutical product" and "new substance" means a medicine containing an active ingredient, or a substance, having a chemical formula which has not previously been marketed or registered in Hong Kong under some other name or description.
L.N. 369/80.
Application for
registration
under section
28A.
Eighth Schedule,
Form 13.
Ninth Schedule.
Eighth Schedule, Form 14.
PART VIIIA
REGISTRATION OF IMPORTERS AND EXPORTERS
37A. (1) Any application for registration under section 28A as an importer or exporter of pharmaceutical products shall be made to the Committee in Form 13 in the Eighth Schedule and shall be accompanied by the fee specified in the Ninth Schedule.
(2) The Committee may require any applicant under this regulation to furnish such information and to permit such inspection of premises and storage facilities used by the applicant for the purposes of his business as the Committee may specify by notice to the applicant.
(3) The Committee may grant or refuse any application under this regulation as the Committee may deem fit.
(4) The Committee shall furnish any person whose application is granted with a certificate in Form 14 in the Eighth Schedule.
(5) Any person aggrieved by a decision of the Committee under this regulation may, in the prescribed manner, appeal to the Tribunal against that decision.
Disclosure of composition of medicines. L.N. 137/78.
PART IX
SALE OF MEDICINES
38. (1) Subject to these regulations, no person shall--- (a) sell any article consisting of or comprising a substance
recommended as a medicine; or
(b) supply any such article as a sample for the purpose of inducing persons to buy the substances of which it consists or which it comprises,
unless-
(i) the article is labelled as required under regulation 31; or
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