In this Order—

• “the 2007 Order” means the Pharmacists and Pharmacy Technicians Order 20074;

• F11“adaptation period” means a period of practice, subject to an assessment and, where necessary, accompanied by further training, which is supervised by a registered pharmacist or registered pharmacy technician;

• “annotation” means an annotation in the Register;

• F11“aptitude test” means an assessment with the aim of determining whether a specified state professional has the knowledge, skills and experience that the Council considers requisite for practising as a registered pharmacist or registered pharmacy technician;

• “assessment team” means an assessment team appointed under rules made under article 55;

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• “controlled drugs” has the meaning given in section 2(1)(a) of the Misuse of Drugs Act 19715 (controlled drugs and their classification);

• “the Council” means the General Pharmaceutical Council established by article 4;

• F6“the Directive” means Directive 2005/36/EC of the European Parliament and of the Council of 7th September 2005 on the recognition of professional qualifications (OJ No L255, 30.09.2005, p 22), and any reference in this Order to the Directive or to any provision of the Directive is a reference to the Directive, or to that provision, as it had effect immediately before IP completion day;

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• “electronic communication” has the meaning given in section 15(1) of the Electronic Communications Act 20007 (general interpretation);

• “enactment” means an enactment contained in, or in an instrument made under—

  1. a

     an Act of Parliament;

  2. b

     an Act of the Scottish Parliament; or

  3. c

     a measure or Act of the National Assembly for Wales;

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• “improvement notice” means a notice served on any person under article 13;

• “individual assessor” means an individual assessor appointed under rules made under article 55;

• “inspector” means an inspector appointed by the Council under article 8(1);

• “medical device” has the meaning given in regulation 2(2) of the Medical Devices Regulations 200210;

• “medicinal product” has the same meaning as it has in the Medicines Act 1968 by virtue of section 130 of that Act11 (meaning of “medicinal product” and related expressions);

• “medicinal product on a general sale list” means a medicinal product of a description, or falling within a class, specified in an order which is for the time being in force under section 51 of the Medicines Act 1968 12(general sale lists);

• F2“the necessary knowledge of English”—

  1. a

     in relation to a person registered, or applying to be registered, as a pharmacist means a knowledge of English which is necessary for the safe and effective practice as a pharmacist in Great Britain;

  2. b

     in relation to a person registered, or applying to be registered, as a pharmacy technician means a knowledge of English which is necessary for the safe and effective practice as a pharmacy technician in Great Britain;

• “the Pharmacy Acts” means the Pharmacy Act 185213, the Pharmacy Act 186814, the Pharmacy Act 190815, the Pharmacy and Poisons Act 193316 and the Pharmacy Act 195417;

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• “prescribed” means prescribed by rules made by the Council;

• F3“professional traineeship” means a period of professional practice, carried out under supervision, that—

  1. a

     constitutes a condition for access to the profession of pharmacist or pharmacy technician in the country in which it is carried out; and

  2. b

     takes place during or after completion of a course of education leading to an educational qualification pursued for the purpose of entry to that profession;

• “the Register” means the register established and maintained under article 19;

• “registered pharmacist” means a person who is entered in Part 1 F8... of the Register;

• “registered pharmacy technician” means a person who is entered in Part 2 F9... of the Register;

• “registered pharmacy” means premises that are entered in Part 3 of the Register;

• “registrant” means a registered pharmacist or a registered pharmacy technician;

• “Registrar”, except where used in the expression “Registrar General”, is to be construed in accordance with article 18(1) and (6);

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• “regulatory body” means a regulatory body which has the function of authorising persons to practise as a member of a health or social care profession;

• “relevant European State” means an EEA State or Switzerland;

• “retail pharmacy business” has the meaning given in section 132 of the Medicines Act 196821 (general interpretation provisions);

• “retail sale” is to be construed in accordance with section 131(3) of the Medicines Act 196822 (meaning of “wholesale dealing”, “retail sale” and related expressions);

• “the Society” means the Royal Pharmaceutical Society of Great Britain;

• F11“specified state professional” means a person who holds a specified state qualification;

• F11“specified state qualification” means a qualification in pharmacy or a pharmacy technician qualification awarded in one of the states specified in Schedule 1 to the Recognition of Professional Qualifications and Implementation of International Recognition Agreements (Amendment) Regulations 2023;

• “statutory committees” means the Committees of the Council listed in article 4(6);

• “superintendent pharmacist” means a pharmacist who is a superintendent for the purposes of section 71(1) of the Medicines Act 196823 (business carried on by body corporate); and

• “supply in circumstances corresponding to retail sale” is to be construed in accordance with section 131(4) of the Medicines Act 1968;

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• F10“the UK GDPR” has the same meaning as in Parts 5 to 7 of the Data Protection Act 2018 (see section 3(10) and (14) of that Act).

For the purposes of this Order, a person practises as a pharmacist or a pharmacy technician if, whilst acting in the capacity of or purporting to be a pharmacist or a pharmacy technician, that person undertakes any work or gives any advice in relation to the preparation, assembly, dispensing, sale, supply or use of medicines, the science of medicines, the practice of pharmacy or the provision of healthcare.

For the purposes of articles 34 and 35, “emergency” means an emergency of the type described in subsection (1)(a) of section 19 of the Civil Contingencies Act 200424 (meaning of “emergency”), read with subsection (2)(a) and (b) of that section.