- Deddfwriaeth Ddrafft
This is a draft item of legislation. This draft has since been made as a UK Statutory Instrument: The Human Tissue (Permitted Material: Exceptions) (England) Regulations 2020 No. 521
2.—(1) Paragraphs (2) to (5) specify types of relevant material(1) for the purposes of the definition of “permitted material” in section 3(9) (“appropriate consent”: adults) of the Human Tissue Act 2004.
(2) Subject to paragraphs (3) and (4), the whole or any part of the following is specified—
(a)arm;
(b)brain;
(c)face;
(d)finger;
(e)foot;
(f)forearm;
(g)hand;
(h)leg;
(i)lower leg;
(j)mouth;
(k)nose;
(l)spinal cord;
(m)thigh;
(n)toe;
(o)trachea;
(p)upper arm;
(q)cervix;
(r)clitoris;
(s)embryo (inside the body)(2);
(t)fallopian tube;
(u)foetus;
(v)labia;
(w)ovary;
(x)penis;
(y)perineum;
(z)placenta;
(aa)prostate;
(bb)testicle;
(cc)umbilical cord;
(dd)uterus;
(ee)vagina;
(ff)vulva.
(3) The following is not specified in so far as it is disaggregated from any of the relevant material specified in sub-paragraphs (a) to (p) of paragraph (2)—
(a)artery;
(b)bone;
(c)muscle;
(d)nervous tissue;
(e)skin;
(f)tendon.
(4) The whole or part of the trachea is not specified in so far as it is attached to a lung.
(5) The following types of cells are specified only in so far as all or part of the cells is for use in, or as, an advanced therapy medicinal product—
(a)limbal stem cells;
(b)liver cells;
(c)lung epithelial cells;
(d)pancreatic cells;
(e)renal epithelial cells.
(6) In this regulation, “advanced therapy medicinal product” has the same meaning as in the Human Medicines Regulations 2012(3).
See section 53 of the 2004 Act for the meaning of “relevant material”.
See section 54(6) of the 2004 Act for the meaning of “embryo”. That subsection was substituted by paragraph 24 of Schedule 7 to the Human Fertilisation and Embryology Act 2008 (c. 22).
S.I. 2012/1916, as prospectively amended by S.I. 2019/775 from IP completion day. “IP completion day” is defined in Schedule 1 to the Interpretation Act 1978 (c. 30).
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i Deddfwyd neu y’i Gwnaed): Mae'r wreiddiol fersiwn y ddeddfwriaeth fel ag yr oedd pan gafodd ei deddfu neu eu gwneud. Ni wnaed unrhyw newidiadau i’r testun.
Mae Memorandwm Esboniadol Drafft yn nodi datganiad byr o ddiben Offeryn Statudol Drafft ac yn rhoi gwybodaeth am ei amcan polisi a goblygiadau polisi. Eu nod yw gwneud yr Offeryn Statudol Drafft yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol, ac maent yn cyd-fynd ag unrhyw Offeryn Statudol neu Offeryn Statudol Drafft a gyflwynwyd yn fanwl gerbron y Senedd o Fehefin 2004 ymlaen.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys