STATUTORY INSTRUMENTS.
(Pl. 9807)
S.I. No. 125 of 1993.
I, RUAIRI QUINN, Minister for Enterprise and Employment, in exercise of the powers conferred on me by section 3 of the European Communities Act, 1972 (No. 27 of 1972), and for the purpose of giving effect to Council Regulation (EEC) No. 1768/921 hereby make the following Regulations:
Notice of the making of this Statutory Instrument was published in "Iris Oifigiúil" of 25th June, 1993.
the Controller shall refuse the request.
REQUEST for the grant of a SUPPLEMENTARY PROTECTION
CERTIFICATE (Medicinal Products)
The Applicant(s) named herein hereby request(s) the grant of a Supplementary Protection Certificate on the basis of the information furnished hereunder:
1. Applicant(s)
Name:
Address:
Nationality/Description:
2. Number of the Basic Patent:
3. Title of the invention:
4. Market Authorisation
(i) The following information relates to the first authorisation to place the product, the subject of this request, on the market in Ireland-
Authorisation No. ...................................................................
Authorisation Date .................................................................
(ii) If the information at (i) does not relate to the first authorisation to place the produce, the subject of this request, on the market in the European Community, please state
Country which granted the first such Authorisation.............................
Authorisation No. ......................................................................
Authorisation Date .....................................................................
Identity of product thus authorised:
Legal provision under which such Authorisation took place:
5. Product Identity
(i) Name, brand or trade name or other description by which the product for which a certificate is requested is commonly known:
(ii) Information to satisfy the Controller that the product is protected by the basic patent identified at 2 above:
6. Items accompanying this Request - tick as appropriate
(i) Request fee.
(ii) Copy of the authorisation specified in Article 8 1.(b) of the EC Regulation in which the product is identified, containing in particular the number and date of the authorisation and the summary of the product characteristics listed in Article 4a of Directive 65/65/EEC or Article 5a of Directive 81/851/EEC.
(iii) Where appropriate, the information and a copy of the notice specified in Article 8 1.(c) of the EC Regulation.
7. Authorised Agent
The following is authorised to act as agent in all proceedings connected with the obtaining of a supplementary protection certificate to which this request relates and in relation to any certificate granted:
Name:
Address:
8. Address for Service (if different from that at 7)
Signed on behalf of Applicants(s):
(Note: this Request may be signed by the Applicant(s) or by the Agent authorised in connection with the basic patent. It may also be signed by another Agent provided an authorisation in favour of that Agent is submitted within 3 months after the filing of this Request.)
Date:
£ | |
Fee payable upon filing of a request for a certificate |
75.00 |
SUPPLEMENTARY PROTECTION CERTIFICATE
Council Regulation (EEC) No. 1768/92
In accordance with article 10 (1) of the above Regulation, this Certificate
is granted to ...........................................................................................
in respect of the product .........................................................................
which is protected by patent no. ................................. which was granted
for an invention entitled...........................................................................
This certificate will expire on ....................................
Dated this . . . . day of . . . . . . . . . . .19
Controller of Patents, Designs and Trade Marks
GIVEN under my Official Seal this 5th day of
May, 1993.
RUAIRI QUINN,
Minister for Enterprise and Employment.
EXPLANATORY NOTE
(This note is not part of the Instrument and does not purport to be a legal interpretation.)
These regulations lay down the fees and procedural requirements which apply to requests for supplementary protection certificates and to certificates granted. The regulations are for the purpose of giving full effect to Council Regulation (EEC) No. 1768/92 concerning the creation of a supplementary protection certificate for medicinal products with effect from 2nd January, 1993.
1 O.J. No. L182/1.