- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Gwreiddiol (a wnaed Fel)
Dyma’r fersiwn wreiddiol (fel y’i gwnaed yn wreiddiol).
235.—(1) Regulation 214(1) does not apply to the sale or supply by a person of a prescription only medicine if—
(a)the person is listed in column 1 of Part 1 of Schedule 17;
(b)the prescription only medicine is listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(2) Regulation 214(1) does not apply to the supply by a person of a prescription only medicine if—
(a)the person is listed in column 1 of Part 2 of Schedule 17;
(b)the prescription only medicine is listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(3) Regulation 214(1) does not apply to the administration by a person of a prescription only medicine if—
(a)the person is listed in column 1 of Part 3 of Schedule 17;
(b)the product is a prescription only medicine for parenteral administration listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(4) Regulation 220 does not apply to the sale, supply or offer for sale or supply by a person of a medicinal product if—
(a)the person is listed in column 1 of Part 4 of Schedule 17;
(b)the product is a prescription only medicine or pharmacy medicine listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(5) Regulation 220 does not apply to the supply by a person of a medicinal product if—
(a)the person is listed in column 1 of Part 5 of Schedule 17;
(b)the product is a prescription only medicine or pharmacy medicine listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(6) Regulation 221 does not apply to the sale, supply, or offer for sale or supply by a person of a medicinal product if—
(a)the person is listed in column 1 of Part 4 of Schedule 17;
(b)the product is a medicinal product subject to general sale that is listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
(7) Regulation 221 does not apply to the sale, supply, or offer for sale or supply by a person of a medicinal product if—
(a)the person is listed in column 1 of Part 5 of Schedule 17;
(b)the product is a medicinal product subject to general sale that is listed in the corresponding paragraph in column 2 of that Part; and
(c)the condition specified in the corresponding paragraph in column 3 of that Part is met.
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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 Memoranda Esboniadol yn nodi datganiad byr o ddiben Offeryn Statudol ac yn rhoi gwybodaeth am ei amcan polisi a goblygiadau polisi. Maent yn ceisio gwneud yr Offeryn Statudol yn hygyrch i ddarllenwyr nad oes ganddynt gymhwyster cyfreithiol, ac maent yn cyd-fynd ag unrhyw Offeryn Statudol neu Offeryn Statudol Drafft a gyflwynwyd ger bron 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:
Impact Assessments generally accompany all UK Government interventions of a regulatory nature that affect the private sector, civil society organisations and public services. They apply regardless of whether the regulation originates from a domestic or international source and can accompany primary (Acts etc) and secondary legislation (SIs). An Impact Assessment allows those with an interest in the policy area to understand:
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