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Efforts to develop more standard bench top assays are deserved to be urgently developed for clinical applications

For a full overview of how the Therapeutic Goods Administration treats laboratory peptide and reconstitution supplies in Australia, see our peptide legality and TGA compliance guide

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All SAEs of death, development of signs of critical illness and severe illness requiring hospitalisation, and AEs as described previously will be reported to the Ethics Committees, the Data and Safety Monitoring Board (DSMB) and to the sponsors of the study within 24 hours of awareness of the event, followed by a final report within 10 days