Therapeutic goods are health-related products used for humans. It includes medicines like complementary, over the counter or prescriptions, medical devices like bandages and others like blood products and disinfectants (Grove, 2019).
Section 3 of the Therapeutic Goods Administration Act, 1989 defines 'therapeutic goods' as
Majorly these are products used for humans for diagnosing and curing any disease, ailment, injury; modifying the physiological process; testing the patients for any disease or testing pregnancy (AG, 2020).
Section 23 of the Therapeutic Goods Act, 1989 entails about the registration of therapeutic goods. Under this, an application has to be made in writing to the Secretary and then delivered to the office of the department. The procedure (AG, 2020) -
I would choose this route as it is specified under the act and is a legal procedure to apply for registration.
The three scientific level and claims under the Therapeutic Goods Act, 1989 are (AG, 2011)-
The above claims can only be supported by either traditional evidence or scientific evidence.
These schedules are categorized into 10 categories (AG, 2020)-
Schedules |
Specifications |
Schedule 1 |
Not currently in use |
Schedule 2 |
Pharmacy medicine |
Schedule 3 |
Pharmacist only medicine |
Schedule 4 |
Prescription-only medicine OR prescription animal remedy |
Schedule 5 |
Caution |
Schedule 6 |
Poison |
Schedule 7 |
Dangerous poison |
Schedule 8 |
Controlled drug |
Schedule 9 |
Prohibited substance |
Schedule 10 |
The substance of danger to health as to warrant prohibition of sale, supply and use. |
These are published in Poison Standard and given accreditation only after state or federal legislation.
A clear piece of work is expected from a scientific writer as his piece is supposed to be informative and persuasive. It should be informative because he has to impart the procedure of his research and persuasive because the writer has to convince his readers that the conclusion drawn from his research is adequate to the principles (EWU, 2020).
Grove, A. (2019). Therapeutic goods: A quick guide. Retrieved from https://www.aph.gov.au/About_Parliament/Parliamentary_Departments/Parliamentary_Library/pubs/rp/rp1819/Quick_Guides/TherapeuticGoods
Australian Government. (2020). What are 'therapeutic goods'? Retrieved from https://www.tga.gov.au/what-are-therapeutic-goods
Australian Government. (2020). Administrative information and prescribing information for Australia - Applicable to applications received by the TGA from 9 February 2018. Retrieved from https://www.tga.gov.au/ctd-module-1
Australian government. (2011). Guidelines for levels and kinds of evidence to support indications and claims for non-registerable medicines, including complementary medicines, and other listable medicines. Retrieved from https://www.tga.gov.au/sites/default/files/cm-evidence-claims-1104.pdf
Australian Government. (2020). Scheduling basics. Retrieved from https://www.tga.gov.au/scheduling-basics
Eastern Washington University. (2020). Scientific writing. Retrieved from https://research.ewu.edu/writers_center_sci_writing#:~:text=To%20avoid%20confusing%20the%20reader,helps%20the%20writer%20accomplish%20this.
Remember, at the center of any academic work, lies clarity and evidence. Should you need further assistance, do look up to our Law Assignment Help
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