The Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1996

Contents

1Citation, commencement and interpretation#

(1)These Regulations may be cited as the Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1996 and shall come into force on 1st April 1996.

(2)In these Regulations, “the principal Regulations” means the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994.

2Amendment of regulation 1 of the principal Regulations#

In regulation 1 of the principal Regulations (citation, commencement and interpretation), after paragraph (3) there is added the following paragraph—“4 In Schedule 2, paragraph 3 (interpretation) shall have effect for the purposes of that Schedule.”

3Substitution of Schedule 2 to the principal Regulations#

For Schedule 2 to the principal Regulations (fees for applications for the grant of certificates of registration) there is substituted the following Schedule—“1 In respect of an application which relates to a product prepared from not more than 5 homoeopathic stocks, the fee shall be the amount set out in Column (2) in the Table below opposite the description in Column (1) appropriate to the application.2 In respect of any other application, the fee shall be the amount set out in Column (3) in the Table below opposite the description in Column (1) appropriate to the application.3 In this Schedule—• “application” means an application for the grant of a certificate of registration;• “formulation” does not include the formulation of a homoeopathic stock;• “identical” means—(a) in relation to the formulation of a product, identical as regards the requirements in respect of composition, preparation and testing;(b) in relation to a homoeopathic stock, identical as regards the source, composition and preparation of the stock and the tests which it is required to undergo;• “product” includes a series of products each of which is prepared from identical homoeopathic stocks;• “repeat formulation” means—(a) the formulation of a product which is identical to the formulation of another product—(a) in respect of which the applicant holds a certificate of registration; or(ii) to which the applicant has, by the holder of the certificate of registration which relates to it, been authorised in writing to make reference for the purposes of his application; or(b) where more than one application is made by the same applicant on the same occasion in respect of products of identical formulations, for the purposes of the second and any subsequent of those applications which the licensing authority considers, the formulation of the product to which the first of those applications which is considered by the licensing authority relates;• “repeat stock” means—(a) a homoeopathic stock which is identical to another homoeopathic stock which is used in the preparation of a product—(a) in respect of which the applicant holds a certificate of registration; or(ii) in respect of which another person holds a certificate of registration to which, for the purposes of his application, the applicant has been authorised in writing to make reference by the person (or, if more than one, each of the persons) who supplied information to the licensing authority in connection with the application for the certificate of registration which relates to that product; or(b) where more than one application is made by the same applicant on the same occasion in respect of products prepared from identical homoeopathic stocks, for the purposes of the second and any subsequent of those applications which the licensing authority considers, the homoeopathic stock used in the preparation of the product to which the first of those applications which is considered by the licensing authority relates.1 An application in respect of a product which is both prepared solely from repeat stocks and is of a repeat formulation2 An application in respect of a product which is either—a prepared solely from repeat stocks; orb is of a repeat formulation3 Any other application”

4Amendment of Schedule 4 to the principal Regulations#

In Schedule 4 to the principal Regulations (application of provisions of the Act), in the second entry in Column (2) which is opposite the entry “section 21” in Column (1), for the words “regulation 5(2) of” in both places where they occur there is substituted “regulation 5(4) of”.

Contains public sector information licensed under the Open Government Licence v3.0.

Defined terms · 6

Show every defined term

application
means an application for the grant of a certificate of registration;
identical
means— (a) in relation to the formulation of a product, identical as regards the requirements in respect of composition, preparation and testing;
product
includes a series of products each of which is prepared from identical homoeopathic stocks;
repeat formulation
means— (a) the formulation of a product which is identical to the formulation of another product— (a) in respect of which the applicant holds a certificate of registration;
repeat stock
means— (a) a homoeopathic stock which is identical to another homoeopathic stock which is used in the preparation of a product— (a) in respect of which the applicant holds a certificate of registration;
the principal Regulations
means the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994.

The Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1996

1Citation, commencement and interpretation#

2Amendment of regulation 1 of the principal Regulations#

3Substitution of Schedule 2 to the principal Regulations#

4Amendment of Schedule 4 to the principal Regulations#

Defined terms · 6

Connections

Key facts

History · 1 version

1Citation, commencement and interpretation#

2Amendment of regulation 1 of the principal Regulations#

3Substitution of Schedule 2 to the principal Regulations#

4Amendment of Schedule 4 to the principal Regulations#