“Article 8 Content of the application for a certificate …. 4. Member States may provide that a fee is to be payable upon application for a certificate and upon application for the extension of the duration of a certificate.”
“Article 12 Annual fees Member States may require that the certificate be subject to the payment of annual fees.”
“Article 14 Expiry of the certificate The certificate shall lapse …. (c) if the annual fee laid down in accordance with Article 12 is not paid in time.”
“Article 19 Procedure 1. In the absence of procedural provisions in this Regulation, the procedural provisions applicable under national law to the corresponding basic patent shall apply to the certificate, unless the national law lays down special procedural provisions for certificates. 2. Notwithstanding paragraph 1, the procedure for opposition to the granting of a certificate shall be excluded.”
“Article 22 Repeal Regulation (EEC) No 1768/92, as amended by the acts listed in Annex I, is repealed. References to the repealed Regulation shall be construed as references to this Regulation and shall be read in accordance with the correlation table in Annex II.”
“Supplemental protection certificates 128B.-(1) Schedule 4A contains provision about the application of this Act in relation to supplementary protection certificates and other provision about such certificates. (2) In this Act a “supplementary protection certificate” means a certificate issued under – (a) Council Regulation (EEC) No 1768/92 of18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products, or (b) Regulation (EC) No 1610/96 of the European Parliament and of the Council of23 July 1996 concerning the creation of a supplementary protection certificate for plant protection products.” (a) Council Regulation (EEC) No 1768/92 of18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products, or (b) Regulation (EC) No 1610/96 of the European Parliament and of the Council of23 July 1996 concerning the creation of a supplementary protection certificate for plant protection products.”
“References to patents etc 1.-(1) In the application to supplementary protection certificates of the provisions of this Act listed in sub-paragraph (2) – (a) references to a patent are to a supplementary protection certificate; (b) references to an application or the applicant for a patent are to an application or the applicant – (i) for a supplementary protection certificate, or (ii) for an extension of the duration of a supplementary protection certificate; …. (2) The provisions referred to in sub-paragraph (1) are - section 14(1), (9) and (10) (making of application); section 19(1) (general power to amend application before grant); sections 20A and 20B (reinstatement of applications); section 21 (observations by third party on patentability); section 27 (general power to amend specification after grant); section 29 (surrender of patents); ….” (a) references to a patent are to a supplementary protection certificate; (b) references to an application or the applicant for a patent are to an application or the applicant – (i) for a supplementary protection certificate, or (ii) for an extension of the duration of a supplementary protection certificate; section 14(1), (9) and (10) (making of application); section 19(1) (general power to amend application before grant); sections 20A and 20B (reinstatement of applications); section 21 (observations by third party on patentability); section 27 (general power to amend specification after grant); section 29 (surrender of patents); ….”
“Fees 5. A supplementary protection certificate does not take effect unless: (a) the prescribed fee is paid before the end of the prescribed period, or (b) the prescribed fee and any prescribed additional fee are paid before the end of the period of six months beginning immediately after the prescribed period.” (a) the prescribed fee is paid before the end of the prescribed period, or (b) the prescribed fee and any prescribed additional fee are paid before the end of the period of six months beginning immediately after the prescribed period.”
“Supplementary protection certificates 116. -(1) An application for: (a) a supplementary protection certificate shall be made on Patents Form SP1; and (b) an extension of the duration of a supplementary protection certificate under Article 8 of the Medicinal Products Regulation shall be made on Patents Form SP4. (2) The period prescribed for the purposes of paragraph 5(a) of Schedule 4A to the Act is – (a) three months ending with the start date; or (b) where the certificate is granted after the beginning of that period, three months beginning immediately after the date the supplementary protection certificate is granted. (3) The comptroller must send a notice to the applicant for the certificate – (a) before the beginning of the period of two months immediately preceding the start date; or (b) where the certificate is granted as mentioned in paragraph (2)(b), on the date the certificate is granted. (4) The notice must notify the applicant for the certificate of – (a) the fact that payment is required for the certificate to take effect; (b) the prescribed fee due; (c) the date before which payment must be made; and (d) the start date. (5) The prescribed fee must be accompanied by Patents Form SP2; and once the certificate has taken effect no further fee may be paid to extend the term of the certificate unless an application for an extension of the duration of the certificate is made under the Medicinal Products Regulation. (6) Where the prescribed fee is not paid before the end of the period prescribed for the purposes of paragraph 5(a) of Schedule 4A to the Act, the comptroller shall, before the end of the period of six weeks beginning immediately after the end of that prescribed period, and if the fee remains unpaid, send a notice to the applicant for the certificate. (7) The notice shall remind the applicant for the certificate – (a) that payment is overdue; and (b) of the consequences of non-payment. (8) The comptroller must send the notices under this rule to – (a) the applicant’s address for service; and (b) the address to which a renewal notice would be sent to the proprietor of the basic patent under rule 39(3).” (a) a supplementary protection certificate shall be made on Patents Form SP1; and (b) an extension of the duration of a supplementary protection certificate under Article 8 of the Medicinal Products Regulation shall be made on Patents Form SP4. (a) three months ending with the start date; or (b) where the certificate is granted after the beginning of that period, three months beginning immediately after the date the supplementary protection certificate is granted. (a) before the beginning of the period of two months immediately preceding the start date; or (b) where the certificate is granted as mentioned in paragraph (2)(b), on the date the certificate is granted. (a) the fact that payment is required for the certificate to take effect; (b) the prescribed fee due; (c) the date before which payment must be made; and (d) the start date. (a) that payment is overdue; and (b) of the consequences of non-payment. (a) the applicant’s address for service; and (b) the address to which a renewal notice would be sent to the proprietor of the basic patent under rule 39(3).”
“63. Thus, although the Interpretation Act does not provide for the situation where EU legislation is repealed, the UK courts are required to construe national legislation in accordance with EU legislation so far as is possible. In this case I have no hesitation in holding that the clear intention of Regulation (EC) No. 469/2009 was that it was to replace Regulation (EEC) No. 1768/92 for all purposes and section 128B should be construed as referring to that Regulation.”
“Article 10 – Renewal fees 1. Member States may require that the certificate shall be subject to the payment of renewal fees imposed by the authority referred to in Article 7(1). 2. The failure to pay such fees will result in the lapse of the certificate.”
“This Article states that the Member States may provide that renewal of the certificate will be subject to the payment of a fee. It will be for the Member States to establish the amount if they decide to introduce such fees, failure of which to pay would cause the certificate to lapse.”
“Article 12 77. This Article states that the Member States may provide that renewal of the certificate is subject to the payment of a fee. It is for the Member States to establish the amount if they decide to introduce such fees, failure to pay causing the certificate to lapse.”
“Article 13 Duration of the certificate 1. The certificate shall take effect at the end of the lawful term of the basic patent for a period equal to the period which elapsed between the date on which the application for a basic patent was lodged and the date of the first authorization to place the product on the market in the Community reduced by a period of five years. 2. Notwithstanding paragraph 1, the duration of the certificate may not exceed five years from the date on which it takes effect.”