Regulation 1
Citation and commencement
These Regulations are the Nurses and Midwives (Exemption for Approved Pharmacists) Regulations 2024 and come into operation on 4 September 2024.
/akn/sg/act/sub_leg/1999/NMA-S693-2024
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Quick answer
Nurses and Midwives (Exemption for Approved Pharmacists) Regulations 2024 is Singapore Subsidiary Legislation, cited as Subsidiary Legislation NMA-S693-2024 1999, currently marked in force and first recorded in 1999.
Citation and commencement
These Regulations are the Nurses and Midwives (Exemption for Approved Pharmacists) Regulations 2024 and come into operation on 4 September 2024.
Definitions
In these Regulations —“approved pharmacist” and “approved retail pharmacy” have the meanings given by Part 2 of the Third Schedule to the Health Products (Therapeutic Products) Regulations 2016 (G.N. No. S 329/2016);“influenza vaccination” means an intramuscular injection to introduce a vaccine into the body of an individual for the purpose of providing the individual protection against influenza.
“approved pharmacist” and “approved retail pharmacy” have the meanings given by Part 2 of the Third Schedule to the Health Products (Therapeutic Products) Regulations 2016 (G.N. No. S 329/2016);
“influenza vaccination” means an intramuscular injection to introduce a vaccine into the body of an individual for the purpose of providing the individual protection against influenza.
Persons who may carry out influenza vaccinations
For the purposes of section 27(6)(c) of the Act, section 27(1) of the Act does not apply to an approved pharmacist who carries out an influenza vaccination at an approved retail pharmacy in accordance with the conditions specified in item 4 of Part 1 of the Third Schedule to the Health Products (Therapeutic Products) Regulations 2016.
For the purposes of section 28(4)(c) of the Act, section 28(1) of the Act does not apply to the employment of an approved pharmacist to carry out an influenza vaccination at an approved retail pharmacy in accordance with the conditions specified in item 4 of Part 1 of the Third Schedule to the Health Products (Therapeutic Products) Regulations 2016.