Title, commencement, application and interpretation

1.—(1) The title of these Regulations is as the Mental Capacity Act 2005 (Loss of Capacity during Research Project) (Wales) Regulations 2007 and they come into force on —

(a) 1 July 2007 for the purpose of enabling applications for approval for the purposes of Schedule 1 to be made to, and determined by, an appropriate body,

(b) 1 October 2007 for all other purposes.

(2) These Regulations apply in relation to Wales.

(3) In these Regulations—

“the Act” (“y Ddeddf”) means the Mental Capacity Act 2005;

“appropriate body” (“corff priodol”) has the meaning given by section 30(4) of the Act and the Mental Capacity Act 2005 (Appropriate Body) (Wales) Regulations 2007(2).

“P” has the meaning given in regulation 2;

“R” has the meaning given in regulation 3.

Application

2.  These Regulations apply where—

(a) a person (“P”) has consented before 31 March 2008 to take part in a research project (“the project”) begun before 1 October 2007; but

(b) before the conclusion of the project, P loses capacity to consent to continue to take part in it, and

(c) research for the purposes of the project in relation to P would, apart from these Regulations, be unlawful by virtue of section 30 of the Act.

Research which may be carried out despite a participant’s loss of capacity

3.  Despite P’s loss of capacity, research for the purposes of the project may be carried out using information or material relating to P if—

(a) the project satisfies the requirements set out in Schedule 1;

(b) all the information or material relating to P which is used in the research was obtained before P’s loss of capacity;

(c) that information or material is either—

(i) data within the meaning of section 1 of the Data Protection Act 1998, or

(ii) material which consists of and/or includes human cells or human DNA; and

(d) the person conducting the project (“R”) takes in relation to P such steps as are set out in Schedule 2.

Regulation 3

SCHEDULE 1 Requirements which the project must satisfy

1.  A protocol approved by an appropriate body and having effect in relation to the project makes provision for research to be carried out in relation to a person who has consented to take part in the project but loses capacity to consent to continue to take part in it.

2.  The appropriate body must be satisfied that there are reasonable arrangements in place for ensuring that the requirements of Schedule 2 will be met.

Regulation 3

SCHEDULE 2 Steps which the person conducting the project must take

1.  R must take reasonable steps to identify a person who—

(a) otherwise than in a professional capacity or for remuneration, is engaged in caring for P or is interested in P’s welfare, and

(b) is prepared to be consulted by R under this Schedule.

2.  If R is unable to identify such a person R must, in accordance with guidance issued by the appropriate authority, nominate a person who—

(a) is prepared to be consulted by R under this Schedule, but

(b) has no connection with the project.

3.  R must provide the person identified under paragraph 1, or nominated under paragraph 2, with information about the project and ask that person—

(a) for advice as to whether research of the kind proposed should be carried out in relation to P, and

(b) what, in that person’s opinion, P’s wishes and feelings about such research being carried out would be likely to be if P had capacity in relation to the matter.

4.  If, any time, the person consulted advises R that in his or her opinion P’s wishes and feelings would be likely to lead P to wish to withdraw from the project if he or she had capacity in relation to the matter, R must ensure that P is withdrawn from it.

5.  The fact that a person is the donee of a lasting power of attorney given by P, or is P’s deputy, does not prevent that person from being the person consulted under paragraphs 1 to 4.

6.  R must ensure that nothing is done in relation to P in the course of the research which would be contrary to—

(a) an advance decision of P’s which has effect, or

(b) any other form of statement made by P and not subsequently withdrawn,

of which R is aware.

7.  The interests of P must be assumed to outweigh those of science and society.

8.  If P indicates (in any way) that he or she wishes the research in relation to him or her to be discontinued, it must be discontinued without delay.

9.  The research must be discontinued without delay if at any time R has reasonable grounds for believing that one or more of the requirements set out in Schedule 1 is no longer met or that there are no longer reasonable arrangements in place for ensuring that the requirements of this Schedule are being met in relation to P.

10.  R must conduct the research in accordance with the provision made in the protocol referred to in paragraph 1 of Schedule 1 for research to be carried out in relation to a person who has consented to take part in the project but loses capacity to consent to take part in it.