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452 result(s) found, displaying 51 to 75
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Presentation: NATA TGA IVD information session 1 - Refresher: Regulatory framework for in-house IVDs
PresentationsThis presentation describes the data requirements and the assessment approach need for in-house IVDs, including Companion Diagnostics. -
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PresentationsWatch our webinar that provides information for prescribers on the vaping reforms, in partnership with the Royal Australian College of General Practitioners (RACGP) and Quit Centre,
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WebinarsThis webinar provides information on the TGA’s public consultation on the impacts, challenges and opportunities relating to medicine shortages.
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Committee meetingsAdvisory Committee on Medical Devices (ACMD) meeting
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Committee meetingsAdvisory Committee on Medicines (ACM) meeting
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WebinarsLearn about vaping reforms and how these will impact consumers, suppliers and health professionals.
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Committee meetingsAdvisory Committee on Medical Devices (ACMD) meeting
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Committee meetingsAdvisory Committee on Medicines (ACM) meeting
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WebinarsWe provided an update on the Australian UDI implementation and a guest speaker presented on the real-world benefits of the UDI adoption in the US healthcare system. See the slides and video.
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Committee meetingsAdvisory Committee on Biologicals (ACB) meeting
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Committee meetingsAdvisory Committee on Complementary Medicines (ACCM) meeting
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Committee meetingsAdvisory Committee on Medical Devices (ACMD) meeting
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WebinarsUpdate on what we know so far, next 6 - month plan and what you can do to get involved.
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Committee meetingsTherapeutic Goods Advertising Consultative Committee
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WebinarsLearn about the new Medical Device Vigilance Program that we will be piloting, and volunteer to participate.
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Committee meetingsAdvisory Committee on Biologicals (ACB) meeting
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WebinarsWebinar to understand recent changes to safety issue reporting requirements as outlined in the Pharmacovigilance responsibilities of medicine sponsors guidance.
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Committee meetingsAdvisory Committee on Medical Devices (ACMD) meeting
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WebinarsAttend this webinar to understand recent changes to safety issue reporting requirements as outlined in the Pharmacovigilance responsibilities of medicine sponsors guidance.
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WebinarsRegister to hear insights from our Good Clinical Practice Inspection Program.
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WebinarsThis presentation provides an update on the GCP Inspection Program implemented in 2022.