If this procedure confirms the initial , the Member State or Switzerland having introduced the procedure shall register the low-risk biocidal product concerned.

[Initial Term of the International ] The international registration shall be effected for an initial term of five years counted from the date of the international registration.

[Renewal of the International ] The international registration may be renewed for additional terms of five years, in accordance with the prescribed procedure and subject to the payment of the prescribed fees.

[International ] The International Bureau shall register each industrial design that is the subject of an international application immediately upon receipt by it of the international application or, where corrections are invited under Article 8, immediately upon receipt of the required corrections.

This also means that before a first , the environmental verifier has to visit all sites at a multi-site organisation.

For such , the competent authorities of the third country concerned must rely on a complete file containing data on the efficacy and innocuity of the vaccine; for imported vaccines the competent authorities may rely on data checked by the competent authorities of the country where the vaccine is produced, as far as these checks have been carried out in conformity with OIE standards.

In considering whether to grant a , the competent authority shall take into account the competence and integrity of the applicant, in particular the absence of any serious infringement or repeated infringements of legislation in the field of drug precursors and the absence of a record of any serious criminal offence.

When considering whether to grant , the competent authorities shall take into account, in particular, the competence and integrity of the applicant.

For such , the competent authorities must rely on a complete file containing data about efficacy and innocuity; for imported vaccines the competent authorities may rely on data checked by the competent authorities of the country where the vaccine is produced, as far as these checks have been carried out in conformity with internationally accepted standards.

Where an organisation applies for , the Competent Body shall register that organisation and give it a registration number if all the following conditions are fulfilled:

Where the Community trade mark application is withdrawn or the Community trade mark ceases to have effect as a result of a surrender being recorded or of failure to renew the , the request for conversion shall be filed within three months after the date on which the Community trade mark application has been withdrawn or on which the Community trade mark ceases to have effect.

Member States should also remain free to fix the provisions of procedure concerning the , the revocation and the invalidity of trade marks acquired by registration.

For , the person identified shall be consistent with the information on the identity of the manufacturer or importer provided in the registration.

In September 2012 by Commission Regulation (EU) No 875/2012 [5], the Commission initiated an investigation concerning the possible circumvention of anti-dumping measures imposed by Council Implementing Regulation (EU) No 990/2011 [6] on imports of bicycles originating in the PRC by imports of bicycles consigned from Indonesia, Malaysia, Sri Lanka and Tunisia, whether declared as originating in Indonesia, Malaysia, Sri Lanka and Tunisia or not, and making such imports subject to (‘the anti-circumvention investigation’).

In 25 September 2012, by Regulation (EU) No 875/2012 [10], the Commission initiated an investigation concerning the possible circumvention of anti-dumping measures imposed by Implementing Regulation (EU) No 990/2011 on imports of bicycles originating in the PRC by imports of bicycles consigned from Indonesia, Malaysia, Sri Lanka and Tunisia, whether declared as originating in Indonesia, Malaysia, Sri Lanka and Tunisia or not, and making such imports subject to (‘the anti-circumvention investigation’).

On agreement on the sharing of the information, the previous registrant shall make available to the new registrant the agreed information and shall give the new the permission to refer to the previous registrant's full study report.

For the purposes of , the format of the technical dossier referred to in Article 10(a) shall be IUCLID.

For , the supplier shall:

However, where a Member State provides for mandatory , the authority or person referred to in the first subparagraph shall take all the measures necessary to ensure such registration.

In the anti-dumping complaint and request for , the evidence regarding export prices from both countries, based on Eurostat data, covers the period from April 2011 to March 2012. The evidence regarding normal value, contained in the anti-dumping complaint and request for registration, consists for both countries of domestic prices.