Prescribed information, content and form of documentE+W

4.—(1) A relevant document must consist of 4 parts as follows—

(a)Part 1, containing a statement summarising the provider's M1 view of the quality of [F1relevant health services] provided or sub-contracted by the provider during the reporting period and the statement referred to in regulation 6;

(b)Part 2, containing the information relevant to the quality of [F2relevant health services] provided or sub-contracted by the provider during the reporting period which is prescribed for the purposes of section 8(1) or (3) of the 2009 Act by [F3paragraphs (2) and (2A)] and the information required by regulation 7;

(c)Part 3, containing other information relevant to the quality of [F4relevant health services] provided or sub-contracted by the provider during the reporting period which is included in the document by the provider; and

(d)an annex containing the statements or copies of the statements referred to in regulation 5.

(2) The information prescribed for the purposes of section 8(1) or (3) of the 2009 Act is the information specified [F5in items 1 to 11 of the table in the Schedule as presented in the way specified in column 2 of those items in that table].

[F6(2A) In relation to the bodies listed in subsection (2)(b) and (d) of section 8 of the 2009 Act who are under the duty in section 8(1) of that Act, the information specified in column 1 of items 12 to 26 of the table in the Schedule as presented in the way specified in column 2 of those items in that table is prescribed information for the purposes of those bodies carrying out that duty.]

(3) The annex referred to in paragraph (1)(d) is not required in a draft relevant document supplied under regulations 8 to 10

Textual Amendments

Marginal Citations

M1See section 9(1) of the Health Act 2009 for the meaning of “the provider”.