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The Secretary of State for Health makes these Regulations in exercise of the powers conferred by sections 28D(1A), 28E, 28S, 28V and 126(4) of the National Health Service Act 1977[1]: Citation, commencement, application and interpretation 1. —(1) These Regulations may be cited as the National Health Service (Primary Medical Services) (Miscellaneous Amendments) (No. 2) Regulations 2005 and shall come into force on 6th January 2006. (2) These Regulations apply in relation to England only. (3) In these Regulations—
Amendment of regulation 2 of the GMS Contracts Regulations 2. —(1) Regulation 2(1) (interpretation) of the GMS Contracts Regulations shall be amended as provided in the following paragraphs. (2) In the definition of "batch issue", for "specified in Part 2 of Schedule 1", substitute "set out in respect of form FP10SS batch issue in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004[5]". (3) In the definition of "immediate family member", after "spouse" insert "or civil partner". (4) In the definition of "repeatable prescription", for "specified in Part 1 of Schedule 1", substitute "set out in respect of form FP10SS repeatable prescription (authorising form) in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004". (5) In the definition of "supplementary prescriber"—
(b) in paragraph (b)(iv), for "and", in the second place where it occurs, substitute "or"; (c) after paragraph (b)(iv), insert—
(d) in paragraph (c), after "an annotation" insert "or entry".
Amendment of regulation 5 of the GMS Contracts Regulations
47. —(1) Without prejudice to any separate right one or more medical practitioners may have under regulation 60 of the Pharmaceutical Regulations (arrangements for provision of pharmaceutical services by doctors), a contractor may provide dispensing services to its registered patients under the contract only if it is authorised or required to do so by the Primary Care Trust in accordance with the following provisions of this paragraph or paragraph 49. (2) A Primary Care Trust may authorise or require a contractor to provide dispensing services to a registered patient only if that patient—
(b) has requested the contractor in writing to provide him with dispensing services.
(3) The conditions referred to in sub-paragraph (2)(a) are that the patient—
(b) is resident in a controlled locality at a distance of more than 1.6 kilometres from any pharmacy (other than a distance selling chemist), and all of the conditions in sub-paragraph (4) are satisfied in his case; (c) is resident in a controlled locality and any pharmacy within a distance of 1.6 kilometres from where the patient lives—
(ii) is a distance selling chemist,
and all of the conditions in sub-paragraph (4) are satisfied in his case; or
(4) The conditions referred to in sub-paragraphs (3)(b) and (c) are that—
(ii) the contract under which the patient receives primary medical services;
(b) there is in effect premises approval in relation to the premises from which the contractor will dispense to the patient; and
(5) If a contractor which has been requested to provide dispensing services by a patient who satisfies one of the conditions in sub-paragraph (3)—
(b) does not so apply, within the period of 30 days beginning with the date on which the patient made that request, the Primary Care Trust may, subject to sub-paragraph (7), require the contractor to provide dispensing services to that patient at listed premises in the case of a patient falling within sub-paragraph (3)(b) or (c), or practice premises in the case of a patient falling within sub-paragraph (3)(a), and shall give the contractor notice in writing to that effect.
(6) An application granted by the Primary Care Trust under sub-paragraph (5)(a) shall, with effect from the date of the patient's request to the contractor, enable that contractor to provide dispensing services at listed premises in the case of a patient falling within sub-paragraph (3)(b) or (c) or practice premises in the case of a patient falling within sub-paragraph (3)(a) to that patient, so long as the contract remains in effect.
(b) in the case of a patient to whom sub-paragraph (3)(b), (c) or (d) applies, the patient would not have serious difficulty by reason of distance or inadequacy of means of communication in obtaining drugs, medicines or appliances from a pharmacy.
(8) A Primary Care Trust shall give the contractor reasonable notice—
(b) that, subject to sub-paragraph (9), where a patient no longer satisfies the requirements of sub-paragraph (3), the contractor shall discontinue the provision of dispensing services to that patient.
(9) A notice under sub-paragraph (8)(b)—
(b) shall not be given—
(ii) during the period for bringing an appeal, or pending the determination of any appeal, referred to in regulation 31(9) of the Pharmaceutical Regulations (determination of whether an area is a controlled locality).
(10) A contractor which has been granted the right under this paragraph to provide dispensing services to some or all of its registered patients may provide any necessary dispensing services to a person whom that contractor has accepted as a temporary resident.
(ii) the contract,
in relation to which it wishes the consent to dispense to be granted; and
(ii) whether the application arises because there has been a practice amalgamation and, if so, the names of the contractors participating in the amalgamation.
(2) An application under sub-paragraph (1) shall be determined in accordance with paragraph 48A and regulations 18, 20(2), 33, 34 and 36 to 38 of the Pharmaceutical Regulations (as modified in accordance with sub-paragraph (4)), as though it were an application for outline consent or premises approval under regulation 61 of those Regulations.
(b) in regulation 18(2), for the reference to provisions being "subject to regulations 25, 26 and 65(4)" there were substituted a reference to the provisions being, "subject to paragraph 48D(4)"; (c) in regulations 18(2)(b) and (c), 33(2)(j), and 34(1)(a), for the references to "regulation 61" there were substituted references to this paragraph; (d) in regulations 33(2) and 36(1) and (9), the references to provisions being "subject to regulations 25 and 26" were omitted; (e) for regulation 33(3) there were substituted—
(b) the Local Medical Committee for the locality of that other Primary Care Trust or Local Health Board (if any); (c) any person whose name is included in the pharmaceutical list of that other Primary Care Trust or Local Health Board, and whose interests might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (d) any LPS chemist in the locality of that other Primary Care Trust or Local Health Board whose interests might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (e) any person (except that other Primary Care Trust or Local Health Board) who is a provider of primary medical services or whose name is included in the dispensing contractor list, or dispensing doctor list maintained in accordance with regulation 68 of the Pharmaceutical Regulations, of that other Primary Care Trust or Local Health Board who might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (f) any Patients' Forum or Community Health Council serving the area of that other Primary Care Trust or Local Health Board; and (g) any other patient, consumer or community group in the area of that other Primary Care Trust or Local Health Board that the Primary Care Trust considers has an interest in the provision of dispensing services in the neighbourhood.";
(f) in regulation 38(2)(c), for the references to "regulation 60" there were substituted a reference to paragraph 47;
(5) Any reference in paragraphs 48A, 48C, 48D or 49A to regulations 18, 20(2), 33, 34 and 36 to 38 shall apply as modified by sub-paragraph (4).
(b) in relation to premises to which sub-paragraph (4) applies, in accordance with sub-paragraphs (11) to (13).
(3) This sub-paragraph applies to premises for which consent to dispense is sought and—
(ii) in a reserved location; or
(b) in relation to which, on the day before the date on which the application for consent to dispense is granted, there are no outstanding applications.
(4) This sub-paragraph applies where, on the day before the date on which the application for outline consent is granted, there are outstanding applications.
(b) which—
(ii) has been granted but the provision of pharmaceutical services from those premises has not commenced.
(6) Where sub-paragraph (2)(b) applies, notification of the determination of the application for consent to dispense by the Primary Care Trust or, on appeal, by the Secretary of State, shall give details of—
(b) the earliest date on which an application can be made under sub-paragraph (11) to the Primary Care Trust for a determination that the consent to dispense should come into effect ("provisional date").
(7) The provisional date is the day after the end of a period of one year beginning with the date of—
(b) where that determination is the subject of an appeal, the determination of that appeal.
(8) The Primary Care Trust may, at any time before the provisional date, for good cause determine that the provisional date shall be extended for a period not exceeding three months beginning with the date specified in sub-paragraph (7)(a) or (b), and any reference in this paragraph or in paragraph 48C to the provisional date shall include a reference to the provisional date as extended under this sub-paragraph.
(b) notify that contractor if any outstanding application is withdrawn; and (c) where it extends the provisional date under sub-paragraph (8), notify that contractor of the new provisional date.
(10) The consent to dispense shall lapse if, before the provisional date, pharmaceutical services are provided from premises which were the subject of an outstanding application which has been granted.
(b) the Primary Care Trust shall determine the request as soon as practicable and in accordance with sub-paragraphs (12) and (13).
(12) Where, on the date of the determination under sub-paragraph (11), the premises are practice premises, the Primary Care Trust shall determine that the consent to dispense and premises approval in respect of those premises shall come into effect on that date.
(b) where none of the premises for which premises approval has been granted are practice premises, the consent to dispense shall lapse.
(14) The Primary Care Trust shall notify its determination under sub-paragraph (11) to the contractor and those persons to whom notice of the application under paragraph 48 was required to be given under regulation 33(2) and (3) of the Pharmaceutical Regulations.
(b) the application for consent to dispense shall be refused under sub-paragraph (13)(a); or (c) consent to dispense shall lapse under sub-paragraph (13)(b),
the contractor may appeal to the Secretary of State against any such determination by giving notice of appeal in accordance with regulation 38(5) of the Pharmaceutical Regulations, and such appeal shall be determined in accordance with regulation 38 of the Pharmaceutical Regulations.
(b) where more than 12 months have elapsed since the last provision of drugs and appliances under an arrangement made pursuant to paragraph 47; (c) in accordance with paragraph 48A(10) or (13); (d) where there is a practice amalgamation and following the amalgamation there are no practice premises which have premises approval; or (e) where the contract has terminated[7].
(2) Premises approval shall cease to have effect in relation to—
(b) listed premises which have not been used for dispensing by the contractor for six months or such longer period as the Primary Care Trust may for good cause allow; (c) listed premises which were granted premises approval under paragraph 48E(3), where no practice amalgamation takes place within the period specified in paragraph 48E(7).
(3) Premises approval shall cease to have effect where the related consent to dispense ceases to have effect.
(b) before the provisional date, the contractor intends to change the premises from which he wishes to dispense,
the contractor may apply to the Primary Care Trust in writing for the Primary Care Trust to determine whether premises approval should be given in relation to the new premises, and the Primary Care Trust shall make the determination in accordance with sub-paragraph (2).
(b) this paragraph and paragraph 48 and regulations 18, 20(2), 34, 36(1) and (3) to (9), 37 and 38 of the Pharmaceutical Regulations shall apply to such an application as they apply to an application for consent to dispense under paragraph 48.
(2) For the purposes of this paragraph—
(b) the "relevant Primary Care Trust" is the Primary Care Trust in whose area the additional premises are situated.
(3) A contractor wishing to be granted premises approval in relation to premises ("new premises") where it wishes to dispense instead of listed premises may apply to all the appropriate Primary Care Trusts and the application shall be determined by the relevant Primary Care Trust in accordance with sub-paragraph (4).
(ii) the Primary Care Trust is otherwise satisfied that granting the application would not result in a significant change in the arrangements for the provision of pharmaceutical services or dispensing services in any part of a controlled locality,
provided that no further applications shall be granted under this sub-paragraph for a period of 12 months beginning with the date on which the contractor commenced providing services from the new premises unless the Primary Care Trust shall for good cause allow; and
(5) The relevant Primary Care Trust shall notify its determination under sub-paragraph (4)(a) to the persons to whom the notice is required to be given under regulation 33(2) and (3) of the Pharmaceutical Regulations and to the appropriate Primary Care Trusts.
(b) where such an appeal is made, the date on which the Secretary of State gives notice of his decision under regulation 38 of the Pharmaceutical Regulations.
(8) Where—
(b) in relation to the premises for which the approval is granted there was, at the date of the grant, an outstanding application,
the premises approval shall provisionally take effect on the date which is the day after the end of a period of one year, or such longer period (not exceeding three months) as the relevant Primary Care Trust may for good cause allow before the expiration of that year, from the final resolution of any outstanding application.
(b) state the period during which the temporary premises approval is to apply; and (c) include those premises in the dispensing contractors list in relation to that contractor.
(10) Temporary premises approval may be granted for a period not exceeding 12 months, and may be renewed for a further period not exceeding three months.
(b) new premises where the premises approval is required for new premises as defined in paragraph 48D(3),
and the Primary Care Trust may grant temporary premises approval under paragraph 48D(9).
(b) the contractor shall have temporary premises approval from the date of the practice amalgamation to dispense from any premises mentioned in the application for a period stated by the Primary Care Trust not exceeding one year.
(5) When the practice amalgamation takes effect the contractor shall notify all Primary Care Trusts in whose area the amalgamated practice is situated that the practice amalgamation has taken place.
(b) to—
(ii) a patient who is not mentioned in sub-paragraph (i) but who is mentioned in paragraph 47(3)(a) or (d) and for whom the contractor making the application is authorised to provide dispensing services on the date the application was refused.
(10) For the purposes of sub-paragraph (9), paragraph 47(3)(b) or (c) shall be read as if the words "and all of the conditions in sub-paragraph (4) are satisfied in his case" were omitted.
(b) the contractor has notified the Primary Care Trust before entering into the contract that it intends to provide dispensing services under it.
(2) In a case to which this paragraph applies the contractor shall be regarded as—
(ii) who wishes the contractor to continue to provide him with such services;
(b) having been granted consent to dispense in relation to the contract under paragraph 48 in relation to the area for which it had such consent under the section 28C arrangements; and
Transitional provisions
(b) premises in addition to or in place of the premises specified in paragraph (a) where, immediately before 6th January 2006, the contractor intended to dispense.
(3) The Primary Care Trust shall determine whether or not to grant premises approval to relevant premises in accordance with sub-paragraphs (4) to (6).
(b) it may make written representations to the Primary Care Trust in relation to such a determination within the period of 30 days beginning with the date of the Primary Care Trust's notification or such longer period as the Primary Care Trust may for good cause allow.
(5) The Primary Care Trust shall—
(b) consider any representations received from the Committees mentioned in paragraph (a) and the contractor; (c) determine that the contractor has premises approval for premises which are, or are part of, relevant premises; and (d) notify its decision to the contractor, the Committees mentioned in paragraph (a), any person providing pharmaceutical services or dispensing services in the Primary Care Trust's area whose interests might, in the opinion of the Primary Care Trust, be affected and all Patients' Forums in that area.
(6) The Primary Care Trust shall grant premises approval under sub-paragraph (3) where it is satisfied that the relevant premises were, prior to 6th January 2006, being routinely used to provide dispensing services.
(b) in paragraph (12), the list of persons to whom notice of the hearing should be sent were a reference to the persons notified under sub-paragraph (5)(d); and (c) in paragraph (14), sub-paragraphs (b), (c) and (d) were omitted.
(9) Until—
(b) the date that any appeal under sub-paragraph (8) is decided,
whichever is the later, a contractor shall be deemed to have been granted premises approval for the relevant premises, but it may not make any application to which paragraph 48C or 48D applies.".
(3) In paragraph 50 (terms relating to the provision of dispensing services), after sub-paragraph (8), insert
(4) In paragraph 51 (dispensing contractor list)—
(b) include the address of the practice premises from which it is authorised or required to dispense; (c) include the premises in relation to which the contractor has premises approval; (d) state in relation to each premises included—
(ii) the date on which premises approval took effect or where it has not taken effect, the date that it was finally granted;
(e) state the area in relation to which there is consent to dispense and premises approval; and
on a list of such contractors (to be called the dispensing contractors list) which it shall prepare, maintain and publish."; and
(5) For paragraph 66 (signing of documents), substitute—
(ii) the name of the contractor on whose behalf it is signed; and
(b) that the documents specified in sub-paragraph (3) include the clinical profession of the health care professional who signed the document.
(2) The documents referred to in sub-paragraph (1)(a) are—
(b) any other clinical documents, apart from those specified in sub-paragraph (3).
(3) The documents referred to in sub-paragraph (1)(b) are batch issues, prescription forms and repeatable prescriptions.".
(6) In paragraph 73 (patient records), in sub-paragraph (4)(c), for ""Good Practice Guidelines for General Practice Electronic Patient Records" published on 26th September 2003", substitute, ""Good Practice Guidelines for General Practice Electronic Patient Records (Version 3.1)" published on 29th July 2005[8]". Amendment of regulation 2 of the PMS Agreements Regulations 8. —(1) Regulation 2 (interpretation) of the PMS Agreements Regulations shall be amended as provided in the following paragraphs. (2) In the definition of "batch issue", for "specified in Part 2 of Schedule 1", substitute "set out in respect of form FP10SS batch issue in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004 [9]". (3) In the definition of "immediate family member", after "spouse" insert "or civil partner". (4) In the definition of "repeatable prescription", for "specified in Part 1 of Schedule 1", substitute "set out in respect of form FP10SS repeatable prescription (authorising form) in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004". (5) In the definition of "supplementary prescriber"—
(b) in paragraph (b)(iv), for "and", in the second place where it occurs, substitute "or"; (c) after paragraph (b)(iv), insert—
(d) in paragraph (c), after "an annotation", insert, "or entry".
Amendment of regulation 5 of the PMS Agreements Regulations
46. —(1) Without prejudice to any separate right one or more medical practitioners may have under regulation 60 of the Pharmaceutical Regulations (arrangements for provision of pharmaceutical services by doctors), a contractor may provide dispensing services to its registered patients under the agreement only if it is authorised or required to do so by the Primary Care Trust in accordance with the following provisions of this paragraph or paragraph 48. (2) A Primary Care Trust may authorise or require a contractor to provide dispensing services to a registered patient only if that patient—
(b) has requested the contractor in writing to provide him with dispensing services.
(3) The conditions referred to in sub-paragraph (2)(a) are that the patient—
(b) is resident in a controlled locality at a distance of more than 1.6 kilometres from any pharmacy (other than a distance selling chemist), and all of the conditions in sub-paragraph (4) are satisfied in his case; (c) is resident in a controlled locality and any pharmacy within a distance of 1.6 kilometres from where the patient lives—
(ii) is a distance selling chemist,
and all of the conditions in sub-paragraph (4) are satisfied in his case; or
(4) The conditions referred to in sub-paragraphs (3)(b) and (c) are that—
(ii) the agreement under which the patient receives primary medical services;
(b) there is in effect premises approval in relation to the premises from which the contractor will dispense to the patient; and
(5) If a contractor which has been requested to provide dispensing services by a patient who satisfies one of the conditions in sub-paragraph (3)—
(b) does not so apply, within the period of 30 days beginning with the date on which the patient made that request, the Primary Care Trust may, subject to sub-paragraph (7), require the contractor to provide dispensing services to that patient at listed premises in the case of a patient falling within sub-paragraph (3)(b) or (c), or practice premises in the case of a patient falling within sub-paragraph (3)(a), and shall give the contractor notice in writing to that effect.
(6) An application granted by the Primary Care Trust under sub-paragraph (5)(a) shall, with effect from the date of the patient's request to the contractor, enable that contractor to provide dispensing services at listed premises in the case of a patient falling within sub-paragraph (3)(b) or (c), or practice premises in the case of a patient falling within sub-paragraph (3)(a) to that patient, so long as the agreement remains in effect.
(b) in the case of a patient to whom sub-paragraph (3)(b), (c) or (d) applies, the patient would not have serious difficulty by reason of distance or inadequacy of means of communication in obtaining drugs, medicines or appliances from a pharmacy.
(8) A Primary Care Trust shall give the contractor reasonable notice—
(b) that, subject to sub-paragraph (9), where a patient no longer satisfies the requirements of sub-paragraph (3), the contractor shall discontinue the provision of dispensing services to that patient.
(9) A notice under sub-paragraph (8)(b)—
(b) shall not be given—
(ii) during the period for bringing an appeal, or pending the determination of any appeal, referred to in regulation 31(9) of the Pharmaceutical Regulations (determination of whether an area is a controlled locality).
(10) A contractor which has been granted the right under this paragraph to provide dispensing services to some or all of its registered patients may provide any necessary dispensing services to a person whom that contractor has accepted as a temporary resident.
(ii) the agreement,
in relation to which it wishes the consent to dispense to be granted; and
(ii) whether the application arises because there has been a practice amalgamation and, if so, the names of the contractors participating in the amalgamation.
(2) An application under sub-paragraph (1) shall be determined in accordance with paragraph 47A and regulations 18, 20(2), 33, 34 and 36 to 38 of the Pharmaceutical Regulations (as modified in accordance with sub-paragraph (4)), as though it were an application for outline consent or premises approval under regulation 61 of those Regulations.
(b) in regulation 18(2), for the reference to provisions being "subject to regulations 25, 26 and 65(4)" there were substituted a reference to provisions being, "subject to paragraph 47D(4)"; (c) in regulations 18(2)(b) and (c), 33(2)(j) and 34(1)(a) for the references to "regulation 61" there were substituted references to this paragraph; (d) in regulations 33(2) and 36(1) and (9), the references to provisions being "subject to regulations 25 and 26" were omitted; (e) for regulation 33(3) there were substituted—
(b) the Local Medical Committee for the locality of that other Primary Care Trust or Local Health Board (if any); (c) any person whose name is included in the pharmaceutical list of that other Primary Care Trust or Local Health Board, and whose interests might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (d) any LPS chemist in the locality of that other Primary Care Trust or Local Health Board whose interests might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (e) any person (except that other Primary Care Trust or Local Health Board) who is a provider of primary medical services or whose name is included in the dispensing contractors list, or dispensing doctor list maintained in accordance with regulation 68 of the Pharmaceutical Regulations, of that other Primary Care Trust or Local Health Board who might, in the opinion of the Primary Care Trust, be significantly affected if the application were granted; (f) any Patients' Forum or Community Health Council serving the area of that other Primary Care Trust or Local Health Board; and (g) any other patient, consumer or community group in the area of that other Primary Care Trust or Local Health Board that the Primary Care Trust considers has an interest in the provision of dispensing services in the neighbourhood.";
(f) in regulation 38(2)(c), for the references to "regulation 60" there were substituted a reference to paragraph 46;
(5) Any reference in paragraphs 47A, 47C, 47D or 48A to regulations 18, 20(2), 33, 34 and 36 to 38 shall apply as modified by sub-paragraph (4).
(b) in relation to premises to which sub-paragraph (4) applies, in accordance with sub-paragraphs (11) to (13).
(3) This sub-paragraph applies to premises for which consent to dispense is sought and—
(ii) in a reserved location; or
(b) in relation to which, on the day before the date on which the application for consent to dispense is granted, there are no outstanding applications.
(4) This sub-paragraph applies where, on the day before the date on which the application for outline consent is granted, there are outstanding applications.
(b) which—
(ii) has been granted but the provision of pharmaceutical services from those premises has not commenced.
(6) Where sub-paragraph (2)(b) applies, notification of the determination of the application for consent to dispense by the Primary Care Trust or, on appeal, by the Secretary of State, shall give details of—
(b) the earliest date on which an application can be made under sub-paragraph (11) to the Primary Care Trust for a determination that the consent to dispense should come into effect ("provisional date").
(7) The provisional date is the day after the end of a period of one year beginning with the date of—
(b) where that determination is the subject of an appeal, the determination of that appeal.
(8) The Primary Care Trust may, at any time before the provisional date, for good cause determine that the provisional date shall be extended for a period not exceeding three months beginning with the date specified in sub-paragraph (7)(a) or (b), and any reference in this paragraph or in paragraph 47C to the provisional date shall include a reference to the provisional date as extended under this sub-paragraph.
(b) notify that contractor if any outstanding application is withdrawn; and (c) where it extends the provisional date under sub-paragraph (8), notify that contractor of the new provisional date.
(10) The consent to dispense shall lapse if, before the provisional date, pharmaceutical services are provided from premises which were the subject of an outstanding application which has been granted.
(b) the Primary Care Trust shall determine the request as soon as practicable and in accordance with sub-paragraphs (12) and (13).
(12) Where, on the date of the determination under sub-paragraph (11), the premises are practice premises, the Primary Care Trust shall determine that the consent to dispense and premises approval in respect of those premises shall come into effect on that date.
(b) where none of the premises for which premises approval has been granted are practice premises, the consent to dispense shall lapse.
(14) The Primary Care Trust shall notify its determination under sub-paragraph (11) to the contractor and those persons to whom notice of the application under paragraph 47 was required to be given under regulation 33(2) and (3) of the Pharmaceutical Regulations.
(b) the application for consent to dispense shall be refused under sub-paragraph (13)(a); or (c) consent to dispense shall lapse under sub-paragraph (13)(b),
the contractor may appeal to the Secretary of State against any such determination by giving notice of appeal in accordance with regulation 38(5) of the Pharmaceutical Regulations, and such appeal shall be determined in accordance with regulation 38 of the Pharmaceutical Regulations
(b) where more than 12 months have elapsed since the last provision of drugs and appliances under an arrangement made pursuant to paragraph 46; (c) in accordance with paragraph 47A(10) or (13); (d) where there is a practice amalgamation and following the amalgamation there are no practice premises which have premises approval; or (e) where the agreement has terminated[11].
(2) Premises approval shall cease to have effect in relation to—
(b) listed premises which have not been used for dispensing by the contractor for six months or such longer period as the Primary Care Trust may for good cause allow; (c) listed premises which were granted premises approval under paragraph 47E(3), where no practice amalgamation takes place within the period specified in paragraph 47E(7).
(3) Premises approval shall cease to have effect where the related consent to dispense ceases to have effect.
(b) before the provisional date, the contractor intends to change the premises from which he wishes to dispense,
the contractor may apply to the Primary Care Trust in writing for the Primary Care Trust to determine whether premises approval should be given in relation to the new premises, and the Primary Care Trust shall make the determination in accordance with sub-paragraph (2).
(b) this paragraph and paragraph 47 and regulations 18, 20(2), 34, 36(1) and (3) to (9), 37 and 38 of the Pharmaceutical Regulations shall apply to such an application as they apply to an application for consent to dispense under paragraph 47.
(2) For the purposes of this paragraph—
(b) the "relevant Primary Care Trust" is the Primary Care Trust in whose area the additional premises are situated.
(3) A contractor wishing to be granted premises approval in relation to premises ("new premises") where it wishes to dispense instead of listed premises may apply to all the appropriate Primary Care Trusts and the application shall be determined by the relevant Primary Care Trust in accordance with sub-paragraph (4).
(ii) the Primary Care Trust is otherwise satisfied that granting the application would not result in a significant change in the arrangements for the provision of pharmaceutical services or dispensing services in any part of a controlled locality,
provided that no further applications shall be granted under this sub-paragraph for a period of 12 months beginning with the date on which the contractor commenced providing services from the new premises unless the Primary Care Trust shall for good cause allow; and
(5) The relevant Primary Care Trust shall notify its determination under sub-paragraph (4)(a) to the persons to whom the notice is required to be given under regulation 33(2) and (3) of the Pharmaceutical Regulations and to the appropriate Primary Care Trusts.
(b) where such an appeal is made, the date on which the Secretary of State gives notice of his decision under regulation 38 of the Pharmaceutical Regulations.
(8) Where—
(b) in relation to the premises for which the approval is granted there was, at the date of the grant, an outstanding application,
the premises approval shall provisionally take effect on the date which is the day after the end of a period of one year, or such longer period (not exceeding three months) as the relevant Primary Care Trust may for good cause allow before the expiration of that year, from the final resolution of any outstanding application.
(b) state the period during which the temporary premises approval is to apply; and (c) include those premises in the dispensing contractors list in relation to that contractor.
(10) Temporary premises approval may be granted for a period not exceeding 12 months, and may be renewed for a further period not exceeding three months.
(b) new premises where the premises approval is required for new premises as defined in paragraph 47D(3),
and the Primary Care Trust may grant temporary premises approval under paragraph 47D(9).
(b) the contractor shall have temporary premises approval from the date of the practice amalgamation to dispense from any premises mentioned in the application for a period stated by the Primary Care Trust not exceeding one year.
(5) When the practice amalgamation takes effect the contractor shall notify all Primary Care Trusts in whose area the amalgamated practice is situated that the practice amalgamation has taken place.
(b) to—
(ii) a patient who is not mentioned in sub-paragraph (i) but who is mentioned in paragraph 46(3)(a) or (d) and for whom the contractor making the application is authorised to provide dispensing services on the date the application was refused.
(10) For the purposes of sub-paragraph (9), paragraph 46(3)(b) or (c) shall be read as if the words "and all of the conditions in sub-paragraph (4) are satisfied in his case" were omitted.
(b) the contractor has notified the Primary Care Trust before entering into the agreement that it intends to provide dispensing services under it.
(2) In a case to which this paragraph applies the contractor shall be regarded as—
(ii) who wishes the contractor to continue to provide him with such services; and
(b) having been granted consent to dispense in relation to the agreement under paragraph 47 in relation to the area for which it had such consent under the general medical service contract; and
Transitional provisions
(b) premises in addition to or in place of the premises specified in paragraph (a) where, immediately before 6th January 2006, the contractor intended to dispense.
(3) The Primary Care Trust shall determine whether or not to grant premises approval to relevant premises in accordance with sub-paragraphs (4) to (6).
(b) it may make written representations to the Primary Care Trust in relation to such a determination within the period of 30 days beginning with the date of the Primary Care Trust's notification or such longer period as the Primary Care Trust may for good cause allow.
(5) The Primary Care Trust shall—
(b) consider any representations received from the Committees mentioned in paragraph (a) and the contractor; (c) determine that the contractor has premises approval for premises which are, or are part of, relevant premises; and (d) notify its decision to the contractor, the Committees mentioned in paragraph (a), any person providing pharmaceutical services or dispensing services in the Primary Care Trust's area whose interests might, in the opinion of the Primary Care Trust, be affected and all Patients' Forums in that area.
(6) The Primary Care Trust shall grant premises approval under sub-paragraph (3) where it is satisfied that the relevant premises were, prior to 6th January 2006, being routinely used to provide dispensing services.
(b) in paragraph (12), the list of persons to whom notice of the hearing should be sent were a reference to the persons notified under sub-paragraph (5)(d); and (c) in paragraph (14), sub-paragraphs (b), (c) and (d) were omitted.
(9) Until—
(b) the date that any appeal under sub-paragraph (8) is decided,
whichever is the later, a contractor shall be deemed to have been granted premises approval for the relevant premises, but it may not make any application to which paragraph 47C or 47D applies.
(b) has requested the Primary Care Trust in writing to provide him with dispensing services.
(3) The conditions referred to in sub-paragraph (2)(a) are that the patient—
(b) is resident in a controlled locality at a distance of more than 1.6 kilometres from any pharmacy (other than a distance selling chemist); (c) is resident in a controlled locality, and any pharmacy within a distance of 1.6 kilometres from where the patient lives—
(ii) is a distance selling chemist; or
(d) is one to whom paragraph (a) or (b) applies and at the time of the request the patient is living as a member of the household, other than as a temporary resident, of another person in respect of whom the Primary Care Trust has consent to dispense.
(4) A Primary Care Trust which provides dispensing services to some or all of its registered patients may provide any necessary dispensing services to a person whom it has accepted as a temporary resident.".
(5) In paragraph 50 (terms relating to the provision of dispensing services), after sub-paragraph (8) insert—
(6) In paragraph 51(dispensing contractor list)—
(b) include the address of the contractor's premises from which it is authorised or required to dispense; (c) include that the contractor is a contractor providing services under an agreement; (d) include the premises in relation to which the contractor has premises approval; (e) state in relation to each premises included—
(ii) the date on which premises approval took effect or where it has not taken effect, the date that it was finally granted;
(f) state the area in relation to which there is consent to dispense and premises approval; and
in its dispensing contractors list which it prepares and maintains under paragraph 51 of Schedule 6 to the General Medical Services Contracts Regulations (dispensing contractor list)."; and
(7) For paragraph 66 (signing of documents), substitute—
(ii) the name of the contractor on whose behalf it is signed; and
(b) that the documents specified in sub-paragraph (3) include the clinical profession of the health care professional who signed the document.
(2) The documents referred to in sub-paragraph (1)(a) are—
(b) any other clinical documents, apart from those specified in sub-paragraph (3).
(3) The documents referred to in sub-paragraph (1)(b) are batch issues, prescription forms and repeatable prescriptions.".
(8) In paragraph 70 (patient records), in sub-paragraph (5)(c), for ""Good Practice Guidelines for General Practice Electronic Patient Records" published on 26th September 2003", substitute, ""Good Practice Guidelines for General Practice Electronic Patient Records (Version 3.1)" published on 29th July 2005[12]". Amendment of regulation 2 of the Pharmaceutical Regulations 14. —(1) Regulation 2(1) (interpretation) of the Pharmaceutical Regulations shall be amended as provided in the following paragraphs. (2) In the definition of "batch issue", for "specified in Part 2 of Schedule 1 to the GMS Regulations", substitute "set out in respect of form FP10SS batch issue in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004[13]". (3) In the definition of "repeatable prescription", for "specified in Part 1 of Schedule 1 (repeat dispensing forms) to the GMS Regulations", substitute "set out in respect of form FP10SS repeatable prescription (authorising form) in the document issued by the Prescription Pricing Authority entitled "Prescription Form Overprint Specifications – GP System Prescription Overprint Specification", version 1 dated June 2004". 15. Article 105 of the General Medical Services and Personal Medical Services Transitional and Consequential Provisions Order 2004[14] is revoked. Signed on behalf of the Secretary of State Warner Minister of State, Department of Health 1st December 2005 (This note is not part of the Order) These Regulations make amendments to certain regulations relating to primary medical services. Part 2 amends the National Health Service (General Medical Services Contracts) Regulations 2004 ("the GMS Contracts Regulations"). In particular, it:
(b) provides that provisions that relate to a spouse will also relate to a civil partner (regulations 2(3) and 7(7)); (c) amends the definition of a "supplementary prescriber" to add optometrists to the list of those who may be so recognised (regulation 2(5)); (d) provides that a contract may be entered into with a person notwithstanding the fact that they have been removed from office as a trustee for a charity, provided such removal did not take place within the previous 5 years (regulation 3); (e) amends the provision relating to payments under a GMS contract to clarify that payments should be made by either party in accordance with any relevant directions (regulation 4); (f) amends the provisions of Schedule 6 of the GMS Contracts Regulations regarding the provision of dispensing services by contractors (regulations 5 and 7(2), (3) and (4)); (g) updates the reference to the good practice document to which contractors must have regard in connection with patient records (regulation 7(6)).
Part 3 makes amendments to the National Health Service (Personal Medical Services Agreements) Regulations 2004 ("the PMS Agreements Regulations") which mirror those made to the GMS Contracts Regulations. In addition, regulation 13(2) amends the provision concerning seeking the views of the Local Medical Committee in considering whether a contractor has prescribed drugs or appliances in excess of what is reasonably necessary. Notes: [1] 1977 c.49; section 28D was inserted by section 21(1) of the National Health Service (Primary Care) Act 1997 (c.46) ("the 1997 Act") and was amended by the insertion of sub-section (1A) by the Health snd Social Care (Community Health and Standards) Act 2003 (c.43) ("the 2003 Act"); section 28E was inserted by section 22(1) of the 1997 Act and was amended by the Health Act 1999 (c.8) ("the 1999 Act"), section 65(2) and Schedule 5, the Health and Social Care Act 2001 (c.15) ("the 2001 Act"), section 27(5)(a), the National Health Service Reform and Health Care Professions Act 2002 (c.17) ("the 2002 Act"), section 4(3), Schedule 3, paragraph 8 and the 2003 Act, section 177(7) to (11); sections 28S and 28V were inserted by section 175(1) of the 2003 Act; section 126(4) was amended by the National Health Service and Community Care Act 1990 (c.19) ("the 1990 Act"), section 65(2), the 1999 Act, Schedule 4, paragraph 37(6) and the 2001 Act, Schedule 5, paragraph 5(13)(b).back [2] S.I. 2004/291, as amended by S.I. 2004/906 and 2694 and 2005/28 and 893.back [3] S.I. 2004/627, as amended by S.I. 2004/906 and 2694 and 2005/28 and 893.back [4] S.I. 2005/641 as amended by S.I. 2005/1015 and 1501.back [5] The overprint specification can be found at www.ppa.org.uk/ppa/prescform_overspec.htm#gpssback [6] 1989 c.44, as amended by S.I. 2005/848.back [7] Paragraph 48 of Schedule 5 to the National Health Service (Personal Medical Services Agreements) Regulations 2004 (S.I. 2004/627 as amended by S.I. 2004/906 and 2694 and S.I. 2005/28 and 893) makes provision in relation to consent to dispense and premises approval where a contractor moves from a general medical services contract to a personal medical services agreement.back [8] This document is available on the following website address: www.dh.gov.uk/PolicyAndGuidance/OrganisationPolicy/PrimaryCare/PrimaryCareComputing.back [9] The overprint specification can be found at www.ppa.org.uk/ppa/prescform_overspec.htm#gpss.back [10] 1989 c.44, as amended by S.I. 2005/848.back [11] Paragraph 49 of the National Health Service (General Medical Services Contracts) Regulations 2004 (S.I. 2004/291, as amended by S.I. 2004/906 and 2694 and 2005/28 and 893) makes provision in relation to consent to dispense and premises approval where a contractor moves from a personal medical services agreement to a general medical services contract.back [12] This document is available on the following website address: www.dh.gov.uk/PolicyAndGuidance/OrganisationPolicy/PrimaryCare/PrimaryCareComputing.back [13] The overprint specification can be found at www.ppa.org.uk/ppa/prescform_overspec.htm#gpssback [14] S.I. 2004/865. Article 105 was amended by S.I. 2005/518.back
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