ICH GCP E6 (R3) guidelines
About
Registration has now closed for this event . If you would like to attend please email Jackie at acta@acta.au to requist the meeting link.A Must-Attend for Clinical Research Professionals
Join the GCP team from the Therapeutic Goods Administration (TGA) and Dr. Tanya Symons, an internationally recognised GCP expert, for an insightful 90-minute webinar on the latest updates to ICH GCP.
In this webinar, we will:
Set expectations regarding the TGA’s process of adopting the updated guidelines, including sector consultation and estimated timelines.
Give an overview of the critical changes to ICH GCP E6 R3.
Demystify new concepts, such as Quality by Design.
Discuss practical guidance on implementing a flexible and efficient approach to GCP.
Provide ample Q&A time to address your questions.
This session is designed for anyone seeking to understand the updated ICH-GCP E6 R3 guidelines. The revisions in R3 will impact all professionals working in the clinical research industry.
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ICH GCP E6 (R3) guidelines
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