(1) After considering whether to approve a draft high level health claims variation and, if notice calling for submissions is given under section 51, after the submission period, the Authority must:
(a) do one of the following:
(i) approve the draft high level health claims variation;
(ii) reject the draft high level health claims variation; and
(b) prepare a report under this section.
Note: The Board must not delegate its powers to act on behalf of the Authority under paragraph (a)--see section 150.
(2) The report must include each of the following:
(a) the reasons for initially accepting the application;
(b) a summary of the recommendations (if any) of the High Level Health Claims Committee in relation to the application and each draft variation that resulted from the application;
(c) a summary of the submissions (if any) made by members of the Food Regulation Standing Committee in relation to the application and each draft variation that resulted from the application;
(d) a summary of the submissions (if any) received by the Authority within the submission period in response to a notice under section 51, if such notice was given;
(e) the Authority's response to the issues raised in those submissions;
(f) the Authority's reasons for approving the draft variation or rejecting the application.