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Industry Regulations Flashcards

7 cards from real FRACGP practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.

Read the first 7 Industry Regulations flashcards as text
  1. Under Australian law, which authority has the power to suspend or cancel a GP's registration if there are serious concerns about their conduct or competence?

    Answer: The Medical Board of Australia, under AHPRA administration

    The Medical Board of Australia, administered through AHPRA, has the statutory authority to take immediate action including suspension of a practitioner's registration.

  2. A GP is asked to complete a WorkCover certificate of capacity for a patient. Which statement best reflects the GP's regulatory obligations in this context?

    Answer: The GP must only certify what is clinically justified and supported by objective assessment findings

    GPs have a professional and legal obligation to certify only what is clinically justified, ensuring WorkCover certificates accurately reflect the patient's functional capacity.

  3. In Australia, prescribing of Schedule 4 (S4) drugs such as antibiotics and benzodiazepines without a valid reason constitutes what type of breach?

    Answer: A potential breach of the Health Practitioner Regulation National Law and professional standards

    Inappropriate prescribing of S4 drugs can constitute a breach of the National Law and professional standards, potentially resulting in regulatory action by the Medical Board of Australia.

  4. Under the Australian Immunisation Register (AIR) legislation, which practitioners are required to report vaccination events?

    Answer: All vaccination providers, including GPs, nurse practitioners, and pharmacists

    All vaccination providers, including GPs, must report every vaccination administered to the Australian Immunisation Register under the Australian Immunisation Register Act 2015.

  5. A GP practising in a rural area wishes to prescribe medication via telehealth for a patient they have never met in person. What is the key regulatory consideration?

    Answer: The GP must establish a therapeutic relationship and meet prescribing standards, with some drugs having additional restrictions for telehealth prescribing

    GPs prescribing via telehealth must still establish an adequate therapeutic relationship and comply with prescribing standards; certain drugs (e.g., S8 drugs) have additional restrictions.

  6. Which Australian standard governs infection prevention and control in general practice settings, including sterilisation of reusable instruments?

    Answer: AS/NZS 4187:2014 – Reprocessing of reusable medical devices in health service organisations

    AS/NZS 4187:2014 is the Australian and New Zealand standard that specifies requirements for reprocessing (cleaning, sterilising) reusable medical devices in health service settings including general practices.

  7. Under the Therapeutic Goods Act 1989, which category of device describes a standard digital blood pressure monitor used in a GP's office?

    Answer: Class IIa (medium-low risk) medical device

    Electronic blood pressure monitors are generally classified as Class IIa medical devices under the TGA framework, requiring inclusion on the Australian Register of Therapeutic Goods (ARTG).