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The presentations cover topics including: Update from TGA to Sector (A01c) Manufacturing Quality and GMP Clearance (A02) In vitro diagnostic (IVD) medical device - reforms and processes (A05) Finding the way to the ARTG for medical devices (A11) Section 19A vs Section 14/14A: a practical approach to reducing the impact of medicine shortages (A16) Software and AI compliance and reforms (A17) Clinical Trials and Good Clinical Practice (GCP) (B02) Labelling TGO 92 update - non-prescription medicines (B09) Labelling TGO 91 update - prescription medicines (B22) Update from TGAs Pharmacovigilance Branch (B13) Prescription Medicine Authorisation Branch update - Q&A panel session (B16) Real World Evidence (C08) A sincere thank you to the TGA presenters for sharing their expertise at the conference and for making these resources available to the wider community

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