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Get the free Application for a Licence to Supply an S4 and/or S8 Drug

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This document is an application form for obtaining a licence to supply Schedule 4 and/or Schedule 8 drugs as per the Controlled Substances (Poisons) Regulations.
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How to fill out application for a licence

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How to fill out Application for a Licence to Supply an S4 and/or S8 Drug

01
Obtain the Application for a Licence to Supply an S4 and/or S8 Drug form from the relevant health authority.
02
Fill in your personal details, including name, address, and contact information.
03
Specify the type of drug (S4 and/or S8) for which you are applying.
04
Provide details about your qualifications and experience relevant to handling controlled substances.
05
Outline the purpose for which the drugs will be supplied.
06
Include any additional documentation required, such as a copy of your professional registration.
07
Review the completed application for accuracy and completeness.
08
Submit the application form and pay any required fees to the appropriate authority.

Who needs Application for a Licence to Supply an S4 and/or S8 Drug?

01
Healthcare professionals who prescribe, dispense, or supply controlled substances.
02
Pharmacies that intend to stock S4 and/or S8 drugs.
03
Hospitals and healthcare facilities that will use or provide S4 and/or S8 drugs.
04
Researchers conducting studies involving S4 and/or S8 drugs.
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How to renew Select the 'Renew online' button. Select 'Next'. Enter your licence and renewal number as shown on your renewal notice. (If you don't have your renewal number, select 'Don't have?' Select 'Next'. Confirm the details of your licence. Enter your payment details. Read and confirm the declaration.
The MAT Act empowers all health care providers with a standard controlled substance license to prescribe for opioid use disorder (OUD), just as they prescribe other essential medications.
The Misuse of Drugs Regulations 2001 were amended in 2012 to allow nurse and pharmacist independent prescribers to prescribe any controlled drug listed in schedules 2 to 5 for any medical condition within their competence, with the exception of diamorphine, and dipipanone for the treatment of addiction.
Attested copies of educational certificates, experience certificates. Attested copy of the letter of approval by State Drugs Controller. Copy of consent letter, appointment letter or joining letter. Medical certificate from a registered medical practitioner along with the eye fitness certificate.
To be eligible for this authority you must be an authorised practitioner, such as a: medical practitioner. nurse practitioner. midwife practitioner. dentist.
Current reportable medicines are S4 medicines containing codeine, , pregabalin, quetiapine, tramadol, zolpidem, zopiclone, and various benzodiazepines.
​​​​​​​​​​​To prescribe or supply registered Schedule 8 medicines (opioids or ketamine) for pain management, or a Schedule 8 benzodiazepine ( and ), a medical or nurse practitioner may be required to obtain an approval* from the NSW Ministry of Health.
The Medicines and Poisons Act 2014 does not allow veterinary surgeons to write prescriptions with repeats for s8 drugs. Prescriptions with repeats of s4 drugs are permitted. The veterinary surgeons concerned were contacted by an inspector and advised of the legislation regarding prescription writing.

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It is a formal application submitted to regulatory authorities to obtain permission to supply controlled substances classified as Schedule 4 (S4) and Schedule 8 (S8) drugs, which are subject to strict legal regulations.
Individuals or entities that intend to manufacture, supply, or dispense S4 and/or S8 drugs, such as pharmacists, medical practitioners, and healthcare organizations, are required to file this application.
To fill out the application, an applicant must provide personal and business details, including qualifications, premises information, any relevant experience, and the specific drugs to be supplied, along with compliance with legal requirements.
The purpose is to regulate the supply of potentially harmful drugs to ensure they are used safely and responsibly, preventing misuse and protecting public health.
The application must report details such as the applicant's identity, qualifications, business address, types of drugs requested, intended use, storage facilities, and any prior licensing history with controlled substances.
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