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                          • 认证机构类别:认证机构
                            认证服务类别:产品认证
                          • When a substance is intended to be manufactured in the Community by one or more
                            manufacturers and/or imported by one or more importers, and/or is subject to registration
                            under Article 7, the following shall apply.
                            Subject to paragraph 3, the information specified in Article 10(a)(iv), (vi), (vii) and (ix),
                            and any relevant indication under Article 10(a)(viii) shall first be submitted by the one
                            registrant acting with the agreement of the other assenting registrant(s) (hereinafter
                            referred to as "the lead registrant").
                            Each registrant shall subsequently submit separately the information specified in
                            Article 10(a)(i), (ii), (iii) and (x), and any relevant indication under Article 10(a)(viii).
                            The registrants may decide themselves whether to submit the information specified in
                            Article 10(a)(v) and (b) and any relevant indication under Article 10(a)(viii) separately or
                            whether one registrant is to submit this information on behalf of the others.


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