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There are currently no known outstanding effects for the The Blood Safety and Quality Regulations 2005, Section 22.
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22.—(1) Blood establishments shall pay to the Secretary of State such fees as are payable in accordance with paragraphs (2) and (3).
(2) The fees payable pursuant to paragraph (1) by blood establishments in relation to authorisation under regulation 3 are—
(a)in respect of an application for authorisation pursuant to regulation 3, the sum of [F1£2,688];
(b)in respect of an application for approval of a substantial change pursuant to regulation 4(10), the sum of [F2£449]; and
[F3(bb)in respect of the assessment by the Secretary of State of serious adverse events and serious adverse reactions notified by blood establishments, an annual haemovigilance fee calculated in accordance with paragraph (2A); and]
(c)in connection with the holding of an authorisation under regulation 3, an annual fee of the sum of [F4£387].
[F5(2A) The fee payable under paragraph (2)(bb) shall be—
(a)in respect of the reporting year ending on 31st March 2006, £156; and
(b)in respect of each subsequent reporting year, [F6£432].]
(3) Where the Secretary of State carries out an inspection at a site of a blood establishment he may charge the establishment and that establishment shall, if so charged, pay to the Secretary of State a fee calculated in accordance with the following sub-paragraphs—
(a)for a regular inspection of a major site, the sum of [F7£13,153];
(b)for a regular inspection of a standard site, the sum of [F8£8,402];
(c)for a regular inspection of a minor site, the sum of [F9£4,120];
(d)for any other inspection, where the inspector spends at least two hours but no more than one day at the site, [F10£2,353];
(e)for any other where an inspector spends more than one day but less than three days at the inspection site, [F11£6,143]; or
(f)for any other inspection where the inspector spends three days or more at the site, [F12£11,449] .
[F13(3A) In respect of each reporting year in which a hospital blood bank has operated, the person who is responsible for management of that hospital blood bank shall pay to the Secretary of State a fee of [F14£600].
(3B) Subject to [F15paragraphs (3D) and (3E)], in respect of the assessment by the Secretary of State of serious adverse events and serious adverse reactions notified by hospital blood banks [F16or facilities], the person who is responsible for management of a hospital blood bank [F17or facility] shall pay to the Secretary of State an annual haemovigilance fee calculated in accordance with paragraph (3C).
(3C) The fee payable under paragraph (3C) shall be—
(b)in respect of the reporting year ending on 31st March 2006, £156; and
(c)in any other case, [F18£432].
(3D) No fee shall be payable under paragraph (3B) by a person responsible for the management of a hospital blood bank if that person is authorised as a blood establishment under these Regulations.]
[F19(3E) No fee shall be payable under paragraph (3B) by a person responsible for the management of a facility where the facility makes arrangements with a hospital blood bank, pursuant to regulation 12B(5) that the hospital blood bank will report serious adverse reactions and events to the Secretary of State on behalf of the facility.]
(4) Where the Secretary of State carries out an inspection of a hospital blood bank [F20or a facility] he may charge the person responsible for management of the hospital blood bank [F21or the facility] and that person shall, if so charged, pay to the Secretary of State a fee calculated in accordance with paragraph (5).
(5) The fees payable by hospital blood banks [F22or facilities] in respect of inspections are—
(a)where an inspector spends at least two hours but no more than one day at the inspection site, [F23£1,126];
(b)where an inspector spends more than one day but less than three days at the inspection site, [F24£3,071]; or
(c)where the inspector spends three days or more at the inspection site, [F25£5,724].
[F26(5A) Where the Secretary of State carries out an inspection of a contract laboratory, he may charge the person having control of that laboratory and that person shall, if so charged, pay to the Secretary of State a fee calculated in accordance with paragraph (5B).
(5B) Subject to paragraph (5C), the fee payable under paragraph (5A) shall be—
(a)if the laboratory carries out only one type of analytical work, [F27£2,996];
(b)if the laboratory carries out two types of analytical work, [F28£4,494]; and
(c)if the laboratory carries out three types of analytical work, [F29£5,992].
(5C) Where an inspection referred to in paragraph (5A) takes place at the same time as an inspection by a person appointed by the Good Laboratory Practice Monitoring Authority under regulation 3(4) of the Good Laboratory Practice Regulations 1999, for the purposes of ascertaining whether the contract laboratory complies with the principles of good laboratory practice, the fee payable under paragraph (5A) shall be—
(a)if the laboratory carries out only one type of analytical work, [F30£750];
(b)if the laboratory carries out two types of analytical work, [F31£1,875]; and
(c)if the laboratory carries out three types of analytical work, [F32£3,000].
(5D) The types of analytical work referred to in paragraphs (5B) and (5C) are—
(a)physico-chemical analysis,
(b)microbiological analysis including sterility testing, and
(c)biological analysis.]
(6) In this regulation—
[F33“contract laboratory” means a laboratory carrying out testing of blood or blood components on behalf of, and pursuant to a contractual arrangement with—
a blood establishment which is authorised under these Regulations; or
a person responsible for management of a hospital blood bank;]
“major site” means a site at which 60 or more persons are involved in processing and quality assurance of blood or blood components;
“minor site” means a site at which fewer than 10 persons are involved in processing and quality assurance of blood or blood components;
“regular inspection” means an inspection of blood establishment pursuant to regulation 15(1);
“standard site” means a site at which at least 10 but fewer than 60 people are involved in processing and quality assurance of blood or blood components.
(7) [F34Subject to paragraph (7A),] any fee payable under this regulation shall be payable at the following times—
(i)the fee payable pursuant to paragraph (2)(a) in respect of an application for authorisation to operate a blood establishment, and the fee payable pursuant to paragraph (2)(b) in respect of an application to make a substantial change, shall, in each case, be payable at the time the application is made;
(ii)the periodic fee payable pursuant to paragraph (2)(c) shall be payable on the first anniversary of the grant by the Secretary of State of authorisation to operate as a blood establishment, and whilst the blood establishment continues to be authorised to operate as such pursuant to these Regulations, annually thereafter;
[F35(iia)any fee payable pursuant to paragraph (2)(bb) or (3B) shall be payable—
(aa)if it is payable in respect of the reporting year ending on 31st March 2006, on 31st December 2005, and
(bb)if it is payable in respect of any subsequent reporting year, on 30th April during that year;
(iib)the fee payable pursuant to paragraph (3A) shall be payable—
(aa)if it is payable in respect of the reporting year ending on 31st March 2006, on 31st December 2005, and
(bb)if it is payable in respect of any subsequent reporting year, on 30th April following the end of that year;]
(iii)any other fee payable under this regulation shall be payable within fourteen days following written notice from the Secretary of State requiring payment of the fee.
[F36(7A) In the case of a blood establishment granted an authorisation under regulation 4 before 8th November 2005, the periodic fee payable pursuant to paragraph (2)(c) shall be payable on 8th November 2006 and, while the blood establishment continues to be authorised to operate as such pursuant to these Regulations, annually thereafter.]
(8) All unpaid sums due by way of, or on account of, any fees payable under this regulation shall be recoverable as debts due to the Crown.
(9) The Secretary of State may in exceptional circumstances where it appears to him to be in the interests of safety or otherwise appropriate to do so—
(a)waive any fee or reduce any fee or part of a fee otherwise payable under this regulation; or
(b)refund the whole or part of any fee paid pursuant to this regulation.
Textual Amendments
F1Word in reg. 22(2)(a) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(2)(a)
F2Word in reg. 22(2)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(2)(b)
F3Reg. 22(2)(bb) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(2)
F4Word in reg. 22(2)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(2)(c)
F5Reg. 22(2A) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(3)
F6Word in reg. 22(2A)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(3)
F7Word in reg. 22(3)(a) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(a)
F8Word in reg. 22(3)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(b)
F9Word in reg. 22(3)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(c)
F10Word in reg. 22(3)(d) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(d)
F11Word in reg. 22(3)(e) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(e)
F12Word in reg. 22(3)(f) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(4)(f)
F13Reg. 22(3A)-(3D) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(4)
F14Word in reg. 22(3A) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(5)
F15Words in reg. 22(3B) substituted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(a)(i)
F16Words in reg. 22(3B) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(a)(ii)
F17Words in reg. 22(3B) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(a)(iii)
F18Word in reg. 22(3C)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(6)
F19Reg. 22(3E) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(b)
F20Words in reg. 22(4) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(c)(i)
F21Words in reg. 22(4) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(c)(ii)
F22Words in reg. 22(5) inserted (31.8.2006) by The Blood Safety and Quality (Amendment) Regulations 2006 (S.I. 2006/2013), regs. 1(1), 14(d)
F23Word in reg. 22(5)(a) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(7)(a)
F24Word in reg. 22(5)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(7)(b)
F25Word in reg. 22(5)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(7)(c)
F26Reg. 22(5A)-(5D) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(5)
F27Word in reg. 22(5B)(a) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(8)(a)
F28Word in reg. 22(5B)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(8)(b)
F29Word in reg. 22(5B)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(8)(c)
F30Word in reg. 22(5C)(a) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(9)(a)
F31Word in reg. 22(5C)(b) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(9)(b)
F32Word in reg. 22(5C)(c) substituted (1.4.2007) by The Blood Safety and Quality (Amendment) Regulations 2007 (S.I. 2007/604), regs. 1(1), 4(9)(c)
F33Words in reg. 22(6) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(6)
F34Words in reg. 22(7) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(7)(a)
F35Reg. 22(7)(iia)(iib) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(7)(b)
F36Reg. 22(7A) inserted (8.11.2005) by The Blood Safety and Quality (Amendment) (No. 2) Regulations 2005 (S.I. 2005/2898), regs. 1(1), 6(8)
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