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United Kingdom Statutory Instruments |
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You are here: BAILII >> Databases >> United Kingdom Statutory Instruments >> The Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1995 No. 541 URL: http://www.bailii.org/uk/legis/num_reg/1995/uksi_1995541_en.html |
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Statutory Instruments
MEDICINES
Made
3rd March 1995
Laid before Parliament
9th March 1995
Coming into force
1st April 1995
1.-(1) These Regulations may be cited as the Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 1995 and shall come into force on 1st April 1995.
(2) In these Regulations, "the principal Regulations" means the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994(3).
2. For paragraph (4) of regulation 5 (determination of application for certificate) there shall be substituted-
"(4) The licensing authority shall consult the Board before refusing to grant a certificate of registration on the ground set out in paragraph (2)(d) above, or, except in the case of a product to which paragraph (3) above applies, on the ground set out in paragraph (2)(c) above.".
3. In regulation 14 of the principal Regulations (fees for variations of certificates), for "£90" there shall be substitued "£85".
4. In Schedule 2 to the principal Regulations (fees for applications for the grant of certificates)-
(a)in paragraph 1, for "£500" there shall be substituted "£475"; and
(b)in paragraph 2, for "£350" there shall be substituted "£335".
Virginia Bottomley
One of Her Majesty's Principal Secretaries of State,
Department of Health
3rd March 1995
(This note is not part of the Regulations)
These Regulations amend the Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994 ("the principal Regulations") which came into force on 14 February 1994 and introduced a new, simplified registration procedure for the marketing of certain homoeopathic medicinal products for human use.
These Regulations reduce by 5% the fees payable under Part III of the principal Regulations in respect of applications for the grant of (regulation 4), and for variations of (regulation 3), certificates of registration granted under the principal Regulations.
In addition these Regulations remove an anomaly in the principal Regulations. Regulation 5(4) of the principal Regulations prescribes the cases in which the licensing authority must, before refusing to grant a certificate of registration, consult the Advisory Board on the Registration of Homoeopathic Products. Regulation 2 of these Regulations substitutes a new regulation 5(4) of the principal Regulations in order to exclude from that duty to consult the case where a refusal of a certificate is required by virtue of regulation 5(2)(c) of the principal Regulations on the ground that the product has an insufficient degree of dilution within the meaning of regulation 5(3).
