Section 3 Section 2: supplementary
Not yet in force
In section 2, “doctor” means a registered medical practitioner.
For the purposes of section 2(2), the kinds of medical treatment that may be innovative medical treatments include (amongst other things)—
the off-label use of an authorised medicinal product, and
the use of a medicinal product in respect of which no F1UK marketing authorisation is in force.
In subsection (2)(a), the reference to the off-label use of an authorised medicinal product is a reference to the use of the product—
for a purpose other than one for which its use is specified,
in relation to a person who is not within a description of persons for whom its use is specified, or
in any other way in which its use is not specified.
In this section—
“authorised medicinal product” means a medicinal product in respect of which a F2UK marketing authorisation is in force;
“ F3UK marketing authorisation” and “medicinal product” have the same meanings as in the Human Medicines Regulations 2012 (S.I. 2012/1916);
“specified”, in relation to a medicinal product, means specified in its F4UK marketing authorisation.
References in section 2 to medical treatment include references to treatment carried out for the purposes of medical research (but nothing in section 2 is to be read as affecting the regulation of medical research).
Nothing in section 2 applies in relation to treatment which is carried out solely for cosmetic purposes.
Annotations
Textual amendments
- F1
Word in s. 3(2)(b) inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 8 para. 2; 2020 c. 1, Sch. 5 para. 1(1)
- F2
Word in s. 3(4)(a) inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 8 para. 2; 2020 c. 1, Sch. 5 para. 1(1)
- F3
Word in s. 3(4)(b) inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 8 para. 2; 2020 c. 1, Sch. 5 para. 1(1)
- F4
Word in s. 3(4)(c) inserted (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), reg. 1, Sch. 8 para. 2; 2020 c. 1, Sch. 5 para. 1(1)