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There are currently no known outstanding effects for the The European Qualifications (Health and Social Care Professions) (Amendment etc.) (EU Exit) Regulations 2019, Paragraph 47.
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47.—(1) Where, immediately before [F1IP completion day], a person was entitled as mentioned in paragraph 15(2) of Schedule 2A to the 2010 Order, any provision made by or under that Order continues to apply in relation to the person without the amendments made by Part 1 of this Schedule to the provisions relating to the provision of occasional pharmacy services by holders of a European professional card.U.K.
(2) For the purposes of paragraph 15(4)(a) of Schedule 2A to the 2010 Order as it continues to apply by virtue of sub-paragraph (1)—
(a)a European professional card that was transmitted as mentioned in paragraph 15(1)(a) of that Schedule is to be treated as becoming invalid on the expiry of the period of 18 months beginning on the day on which it was transmitted;
(b)a European professional card that was issued as mentioned in paragraph 15(1)(b) of that Schedule is to be treated as becoming invalid on the expiry of the period of 12 months beginning with the day on which it was issued.
(3) The reference in sub-paragraph (1) to “the provisions relating to the provision of occasional pharmacy services by holders of a European professional card” is to the provisions listed in the following table.
Instrument | Provision relating to visiting practitioners |
---|---|
The 1968 Act | section 67E |
section 69(1ZA) | |
section 71(7) | |
section 78(5) and (5A) | |
The 2010 Order | in article 3(1), the definitions of “competent authority”, “European professional card”, “General Systems Regulations”, “IMI”, “IMI file” and “registered pharmacist” |
article 19(2)(d) | |
article 29(3)(a) | |
article 33A | |
article 36(3) | |
article 37(5) | |
article 38(2) and (4) | |
article 39(1)(c), (i) and (l) | |
article 43(5)(c), (8)(b) and (9) | |
in Schedule 2A, paragraphs 2 (except the definitions of “automatically recognised pharmacist”, “EPC holder” and “missing document”), 15 and 16 | |
Medicines for Human Use (Clinical Trials) Regulations 2004 | regulation 2(1) |
National Health Service (Pharmaceutical Services) (Scotland) Regulations 2009 | regulation 2(1) |
General Pharmaceutical Council (Registration) Rules 2010 | rule 18(1)(a) and (5)(a)(i) |
rule 19(1), (4)(a) and (5)(b) | |
rule 20(3)(a) | |
General Pharmaceutical Council (Continuing Professional Development and Consequential Amendments) Rules 2011 | rule 5(2)(b) and (3) |
rule 8(1) | |
rule 9(5) | |
rule 11(1)(a) | |
Human Medicines Regulations 2012 | regulation 8(1) |
National Health Service (Pharmaceutical and Local Pharmaceutical Services) Regulations 2013 | regulation 2(1) |
Textual Amendments
F1Words in Sch. 2 para. 47(1) substituted (31.12.2020 immediately before IP completion day) by The European Qualifications (Health and Social Care Professions) (EFTA States) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1394), regs. 1(2), 10(6)
Commencement Information
I1Sch. 2 para. 47 in force at 31.12.2020 on IP completion day (in accordance with 2020 c. 1, Sch. 5 para. 1(1)), see reg. 1(2)
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