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    13. Forms
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    Contents

    13. Forms

    • 1 Mins to read
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    Article summary

    1. Australian Code for the Responsible Conduct of Research
    2. Safety Monitoring and Reporting in Clinical Trials Involving Therapeutic Goods
    3. Membership profile form (DOCX 50 KB) (not available in pdf)
    4. ToR/SOP requirements form (DOCX 60 KB) (not available in pdf)
    5. Human Research Ethics Application (HREA) How-to Guide
    6. Participant Information Sheet/Consent Form (not available in pdf)
    7. Supply of unapproved therapeutic goods under the clinical trial approval (CTA) scheme - Part 1 The CTA application (docx,134kb) (not in pdf)
    8. Supply of unapproved therapeutic goods under the clinical trial approval (CTA) scheme - Part 2 Notification of the conduct of a trial under the CTA scheme (docx,135kb) (not in pdf)
    9. Payment of Participants in Research
    10. Application for approval to import/export unapproved therapeutic goods for experimental purposes in humans.
    11. Application for approval to import/export unapproved therapeutic goods for experimental purposes (Microsoft Word,129kb)
    12. B319 ICS Client Registration application form (pdf,809kb)
    13. Ethical conduct in research with Aboriginal and Torres Strait Islander Peoples and communities
    14. Module 1.10 Paediatric development program
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