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Pharmacovigilance and complementary medicines - Regulatory requirements
The challenges of regulating direct to consumer digital medical devices
Updates from the Pharmacovigilance and Special Access Branch
Consumer Medicine Information - Improving the CMI template
Regulatory updates from the Complementary and OTC Medicines Branch - Listed medicines regulatory reforms
Improved electronic submission methodologies - Challenges and future state
Regulation, ethics and reimbursement of novel biological therapies in Australia – an update
Updates to Good Manufacturing Practices - Recent, current and future changes
Good Clinical Practice Inspections - Consultation to introduce a pilot program of voluntary GCP inspections
Manufacturing Investigational Medicinal Products - Legislative and GMP requirements
Update on regulatory reforms from the Scientific Evaluation Branch
Update on regulatory reforms from the Scientific Evaluation Branch
Reporting of Medicine Shortages
Regulatory updates from the TGA Medical Devices Branch - Part 1
Regulatory updates from the TGA Medical Devices Branch - Part 2