Events

This webinar provides an overview of TGA’s Good Clinical Practice (GCP) Inspection Program clinical trial compliance activities.

Information session for external stakeholders about the proposed IVD regulation changes.

Are you interested in applying to be a member of one of the TGA’s Statutory Advisory Committees? Hear first-hand from current members and the Chief Medical Adviser about what this exciting role is like.

This is a Q&A Session for Industry about the recently published guidance on listed probiotic medicines.

An overview of the amended sponsor portal to include unapproved medical devices and provides guidance on how to apply for consent to import, supply or export medical devices that do not comply with the Essential Principles (EPs).

Guidance on completing updated notification form for new therapeutic vaping products, and information on the re-statement of compliance when requested by TGA.

See the upcoming changes in the PRAC – the new procedure document that will replace the Uniform Recalls Procedure for Therapeutic Goods (URPTG).

Presentations given by the TGA at the ARCS 2025 Regulatory Summit, 19 February 2025