Singapore legislation
Regulation 2
of Healthcare Services (Outpatient Renal Dialysis Service) Regulations 2023
Regulation 2
Definitions
In these Regulations —“collaborative prescribing practitioner” has the meaning given by regulation 2 of the Healthcare Services (Collaborative Prescribing Service) Regulations 2023 (G.N. No. S 398/2023);“duly qualified allied health professional” has the meaning given by section 3 of the Allied Health Professions Act 2011;“enrolled nurse” means a person who is an enrolled nurse within the meaning of the Nurses and Midwives Act 1999 and holds a valid practising certificate under that Act;“essential life‑saving measure” means any basic emergency procedure that may be carried out on a person for the purpose of resuscitating the person;“expiry date” has the meaning given by regulation 2 of the General Regulations;“General Regulations” means the Healthcare Services (General) Regulations 2021 (G.N. No. S 1035/2021);“haemodialysis” has the meaning given by paragraph 2 of the First Schedule to the Act;“healthcare professional” has the meaning given by regulation 2 of the General Regulations;“health product” has the meaning given by section 2(1) of the Health Products Act 2007;“licensee” means a person who holds a licence to provide an outpatient renal dialysis service;“medicinal product” has the meaning given by section 3 of the Medicines Act 1975;“nursing personnel” means a registered nurse, an enrolled nurse or any other person who assists a registered nurse or an enrolled nurse in providing nursing care to patients;“nursing service” means the provision of nursing care to a patient to assist the patient in attaining, maintaining or recovering his or her health;“outpatient renal dialysis service” has the meaning given by paragraph 2 of the First Schedule to the Act;“peritoneal dialysis” has the meaning given by paragraph 2 of the First Schedule to the Act;“peritoneal dialysis support” has the meaning given by paragraph 2 of the First Schedule to the Act;“personnel”, in relation to a licensee, means any individual employed or engaged by the licensee to assist the licensee in providing the outpatient renal dialysis service;“registered nurse” means a person who is a registered nurse within the meaning of the Nurses and Midwives Act 1999 and holds a valid practising certificate under that Act;“simple in vitro diagnostic test” has the meaning given by paragraph 2 of the First Schedule to the Act;“specified infectious disease” means any of the following infections:
Hepatitis B infection;
Hepatitis C infection;
human immunodeficiency virus infection;“specimen” has the meaning given by regulation 2 of the General Regulations;“supervising nurse”, in relation to an outpatient renal dialysis service, means the person appointed under regulation 9(1) as the supervising nurse for the outpatient renal dialysis service;“temporary premises” means any premises other than permanent premises;“testing material” means any test kit, material, device, equipment, instrument or other article that is used to conduct a simple in vitro diagnostic test.
Definition
“collaborative prescribing practitioner” has the meaning given by regulation 2 of the Healthcare Services (Collaborative Prescribing Service) Regulations 2023 (G.N. No. S 398/2023);
Definition
“duly qualified allied health professional” has the meaning given by section 3 of the Allied Health Professions Act 2011;
Definition
“enrolled nurse” means a person who is an enrolled nurse within the meaning of the Nurses and Midwives Act 1999 and holds a valid practising certificate under that Act;
Definition
“essential life‑saving measure” means any basic emergency procedure that may be carried out on a person for the purpose of resuscitating the person;
Definition
“expiry date” has the meaning given by regulation 2 of the General Regulations;
Definition
“General Regulations” means the Healthcare Services (General) Regulations 2021 (G.N. No. S 1035/2021);
Definition
“haemodialysis” has the meaning given by paragraph 2 of the First Schedule to the Act;
Definition
“healthcare professional” has the meaning given by regulation 2 of the General Regulations;
Definition
“health product” has the meaning given by section 2(1) of the Health Products Act 2007;
Definition
“licensee” means a person who holds a licence to provide an outpatient renal dialysis service;
Definition
“medicinal product” has the meaning given by section 3 of the Medicines Act 1975;
Definition
“nursing personnel” means a registered nurse, an enrolled nurse or any other person who assists a registered nurse or an enrolled nurse in providing nursing care to patients;
Definition
“nursing service” means the provision of nursing care to a patient to assist the patient in attaining, maintaining or recovering his or her health;
Definition
“outpatient renal dialysis service” has the meaning given by paragraph 2 of the First Schedule to the Act;
Definition
“peritoneal dialysis” has the meaning given by paragraph 2 of the First Schedule to the Act;
Definition
“peritoneal dialysis support” has the meaning given by paragraph 2 of the First Schedule to the Act;
Definition
“personnel”, in relation to a licensee, means any individual employed or engaged by the licensee to assist the licensee in providing the outpatient renal dialysis service;
Definition
“registered nurse” means a person who is a registered nurse within the meaning of the Nurses and Midwives Act 1999 and holds a valid practising certificate under that Act;
Definition
“simple in vitro diagnostic test” has the meaning given by paragraph 2 of the First Schedule to the Act;
Definition
“specified infectious disease” means any of the following infections:
Hepatitis B infection;
Hepatitis C infection;
human immunodeficiency virus infection;
Definition
“specimen” has the meaning given by regulation 2 of the General Regulations;
Definition
“supervising nurse”, in relation to an outpatient renal dialysis service, means the person appointed under regulation 9(1) as the supervising nurse for the outpatient renal dialysis service;
Definition
“temporary premises” means any premises other than permanent premises;
Definition
“testing material” means any test kit, material, device, equipment, instrument or other article that is used to conduct a simple in vitro diagnostic test.