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The Patents (Supplementary Protection Certificate for Medicinal Products) (Amendment) Rules 1993 (S.I. 1993/947), United Kingdom

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Latest Version in WIPO Lex
Details Details Year of Version 1993 Dates Adopted: April 21, 1993 Type of Text Implementing Rules/Regulations Subject Matter Patents (Inventions), Plant Variety Protection Notes This text refers to 'Council Regulation (EEC) No. 1768/92 of 18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products' available in the Database as 'Patents (Supplementary Certificate Medicinal Products), Council Regulation, 18/06/1992, No. 1768/92' (EU_013)
The notification by the United Kingdom to the WTO under article 63.2 of TRIPS states:
'The Rules correct certain drafting errors in The Patents (Supplementary Protection Certificate for Medicinal Products) Rules 1992 (S.I. 1992/3162).'

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Main text(s) Main text(s) English The Patents (Supplementary Protection Certificate for Medicinal Products) (Amendment) Rules 1993 (S.I. 1993/947)        
GB080: Patents (No. 1768/92/EEC Certificate Medicinal Products), Rules (Amendment), 30/03/1993, No. 947

This Statutory Instrument has been made in consequence of defects in S.I. 1992/3162 and is being issued free of charge to all known recipients of that Statutory Instrument.

1993 No. 947
PATENTS

The Patents (Supplementary Protection Certificate for
Medicinal Products) (Amendment) Rules 1993

Made

30th March 1993

Laid before Parliament

31st March 1993

Coming into force

21st April 1993

The Secretary of State, in exercise of the powers conferred by section 123 of, and paragraph 14 of Schedule 4 to, the Patents Act 19771, after consultation with the Council on Tribunals pursuant to section 8 (1) of the Tribunals and Inquiries Act 19922, hereby makes the following Rules:-

1.-
(1) These Rules may be cited as the Patents (Supplementary Protection Certificate for Medicinal Products) (Amendment) Rules 1993 and shall come into force on 21st April 1993.
(2) These Rules extend to Great Britain and Northern Ireland.
(a) in the column headed "Reminder" of Form SP1 (Request for grant of Supplementary Protection Certificate) in Schedule 2 (General Forms), the words "must be valid at the time of making the application and" appearing in the second item thereunder shall be omitted;
(b) in Schedule 4 (Fees), for the word "Request" in the first item thereunder there shall be substituted the word "Application" and for the words "On payment of annual fees (and additional fee for late payment)" in the second item thereunder there shall be substituted "Annual fees".

E Leigh
Parliamentary Under Secretary of
State for Trade and Technology
Department of Trade and Industry

30th March 1993

EXPLANATORY NOTE

(This note is not part of the Rules)

These Rules amend the Patents (Supplementary Protection Certificate for Medicinal Products) Rules 1992 (S.I. 1992/3162 which came into force on 2nd January 1993) to correct certain drafting errors in those Rules.

11977 c.37; the power of the Secretary of State to make rules in respect of patents under section 123 of the Patents Act 1977 was extended by the Patents (Supplementary Protection Certificate for Medicinal Products) Regulations 1992 (S.I. 1992/3091) so as to apply in respect of supplementary protection certificates. Section 123 was amended by the Copyright, Designs and Patents Act 1988 (c.48), section 295 and Schedule 5, paragraph 29.

3S.I. 1992/3162.


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