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Dispelling GMP myths of human blood, blood components, tissues, cells and gene therapies
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Disclaimer
This presentation paper is provided on the TGA's website solely for the purpose of indicating or suggesting what TGA representatives spoke about to the various conferences and seminars to which it relates. The paper is not legislative in nature and should not be taken to be statements of any law or policy in any way.
The Australian Government Department of Health (of which the TGA is a part) advises that (a) the presentation paper should not be relied upon in any way as representing a comprehensive description of regulatory requirements, and (b) cannot guarantee, and assumes no legal liability or responsibility for, the accuracy, currency or completeness of the information contained in the presentation paper.
Presentation
- Presented by: Alyce Maksoud and Nadia Saleh
- Presented at: Online
- Presentation date: 13 May 2021
- Presentation summary: An overview of the Australian Biological regulatory framework and the common misconceptions around the GMP requirements.
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