Associated information

Associated information

This page provides links to any policies, procedures, guidelines, legislation, websites or other material identified by the author as having a direct association with the document.

Clinical Trial Governance Procedure

( View Historic Versions )


Legislation
Therapeutic Goods Act 1989
Therapeutic Goods Regulations 1990
Codes
AIATSIS Code of Ethics for Aboriginal and Torres Strait Islander Research
Australian Code for the Responsible Conduct of Research 2018
Documents
  Administration of Research Funding - Applications, Grants and Contract Research Policy
  Animal Ethics in Teaching and Research Procedure
  Authorship Procedure
  Consultancy Procedure
  Consultancy, Secondary Employment and Internal Work Policy
  Enterprise Risk Management Framework Policy
  Export Controls and Sanctions Regimes Procedure
  Higher Degree by Research Candidature Charter Policy
  Human Research Ethics Procedure
  Managing Complaints about the Conduct of Research - Higher Degree by Research Candidates Procedure
  Managing Complaints about the Conduct of Research Procedure
  Open Access for UQ Research Publications Policy
  Research Data Management Policy
  Responsible Research Management Framework Policy
  Secondary Employment and Internal Work Procedure
  Staff Code of Conduct Guideline
  Staff Code of Conduct Policy
  Student Code of Conduct Policy
  Working with Children Policy
Website Links
  Australian Clinical Trial Handbook
  Clinical Trial Risk Assessment and Management Plan Template
  Enterprise Risk
  ICH Guideline for Good Clinical Practice
  Information Governance and Management Framework
  Insurance for Human Research Studies - Declaration For Approval
  Insurance for Human Research Studies - Notification
  Insurance for Human Research Studies/Clinical Trials
  Insurance Services
  ISO 14155:2020 Clinical Investigation of Medical Devices for Human Subjects
  Medicines Australia - Clinical Trial Research Agreements
  Medicines Australia - Indemnity & Compensation Guidelines
  National Mutual Acceptance Scheme for Ethical and Scientific Review of Multi-Centre Research
  National Statement on Ethical Conduct in Human Research
  NHMRC Guidance - Safety Monitoring and Reporting in Clinical Trials involving Therapeutic Goods
  Report an Incident or Hazard
  Research Support - Research Partnerships Managers
  Schedules of Delegation and Sub-delegation
  Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT)
  UQ Safety Network Contacts