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A patient or their medical practitioner or nurse practitioner may approach your pharmacy to assist with dispensing an approved medicinal cannabis product. Products may include both registered and unregistered medicines. Generally, for unapproved medicinal cannabis, only stock for a named patient can be held in a pharmacy. However, a pharmacist may hold stock for an Authorised Prescriber AP but this stock should only be used for that medical practitioners patients. Only registered medical practitioners can become Authorised Prescribers. The Medicines and Poisons Act and Medicines and Poisons Medicines Regulation describes the requirements for dispensing, recording, packaging, labelling and reporting associated with schedule 4 and schedule 8 medicines including medicinal cannabis products. To find out more, read the report on stakeholder feedback, Medicinal cannabis in Queensland — A report on stakeholder feedback — July PDF kB. Importation and export of medicinal cannabis products is tightly controlled. The Office of Drug Control provides information on how to access these products. Medicinal cannabis products, particularly those containing tetrahydrocannabinol THC , have a high diversion value, and must have comprehensive security controls in place to manage this risk. The Departmental Standard — Secure storage of S8 medicines outlines the requirements for storing Schedule 8 medicines, including schedule 8 medicinal cannabis products. If the medicinal cannabis is a schedule 8 medicine, it must be stored in a way that complies with the Departmental Standard — Secure storage of S8 medicines PDF kB. Under the Medicines and Poisons Medicines Regulation , community pharmacies and dispensing medical practitioners that dispense S8 medicinal cannabis are required to submit these dispensing records to QScript electronically via a Prescription Exchange Service PES , along with all other dispensing records for monitored medicines prescriptions. Read more about Monitored medicine reporting requirements. Visit Monitored medicines reporting requirements for further information. The Queensland Government is now in caretaker mode until after the state election. Learn more. Menu Close. Public health and wellbeing. Clinical practice Clinical practice. Clinical practice. Health system and governance. Careers Careers. Research and reports. Newsroom Newsroom. Contact us. Medicinal cannabis Medicinal cannabis Patient information for accessing medicinal cannabis Prescribing medicinal cannabis Guide for pharmacists dispensing medicinal cannabis Clinical trials and other research Regulation and control. Guide for pharmacists dispensing medicinal cannabis. Guidance and regulations In conjunction with the Commonwealth Department of Health and Aged Care, state and territory health departments and universities, guidance documents have been prepared on the use of medicinal cannabis in Australia. This suite of national guidance documents cover a range of medical conditions, symptoms, and products to be used. The individual documents can be viewed on the TGA's website. The Departmental Standard — Secure storage of S8 medicines PDF kB details how to secure and store medicinal cannabis products, under the regulation. Read more about Prescribing and dispensing unapproved medicinal cannabis PDF kB The dispenser must: comply with the Departmental Standard — Monitored medicines PDF kB when dispensing an S8 medicinal cannabis product and check QScript prior to dispensing a monitored medicine, including S8 medicinal cannabis unless an exemption applies or the dispenser has a reasonable excuse. Importation Importation and export of medicinal cannabis products is tightly controlled. Departmental Standard — Secure storage of Schedule 8 medicines Medicinal cannabis products, particularly those containing tetrahydrocannabinol THC , have a high diversion value, and must have comprehensive security controls in place to manage this risk. Read more about Monitored medicine reporting requirements Read more about Prescribing and dispensing unapproved medicinal cannabis PDF kB Visit Monitored medicines reporting requirements for further information. Last updated: 9 October Back to top.
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