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practitioners and emergency care assistants, to administer the listed medicines for the purpose of saving a life in an emergency. Ambulance organisations take responsibility for the safe treatment of their patients by agreeing the practitioner groups who can administer each Schedule 19 medicine.
The HMRs set out a comprehensive regime for the authorisation of medicinal products for human use; for the manufacture, import, distribution, sale and supply of those products; for their labelling and advertising; and for pharmacovigilance.
The Human Medicines Regulations 2012 (the \u201cRegulations\u201d) is the main legislation in the UK covering the manufacture, importation, distribution, advertising, labelling, sale and supply of medical products for human use and pharmacovigilance (the monitoring of the effect and safety of medical drugs after they have been ...
They set out a comprehensive regime for the authorisation of products; for the manufacture, import, distribution, sale and supply of those products; for their labelling and advertising; and for pharmacovigilance.
The Medicines Act 1968 is the legal basis allowing you to administer medication to people you support. The Act states that anyone can administer a prescribed medicine to another person, so long as they follow the directions provided by the prescriber.
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It governs the control of medicines for human use and for veterinary use, which includes the manufacture and supply of medicines, and the manufacture and supply of (medicated) animal feeding stuffs.
List of Schedule 5 (V) Drugs.
EMTs and paramedics administer numerous drugs, like epinephrine for anaphylaxis, for asthma, and nitroglycerine for chest pain, to treat life-threatening medical conditions and relieve patient pain.
The Human Medicines Regulations 2012 defines three legal categories of medicines: General Sales List medicines (GSL) Pharmacy medicines (P) Prescription Only Medicines (POM)
The Health Act 1999, as amended by the Health and Social Care Act 2008, is the primary legislation which enabled the GPhC to be established via the Pharmacy Order 2010. The Act enabled all the regulatory functions of the Royal Pharmaceutical Society of Great Britain to be transferred to the GPhC.

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