TGA vs BfArM: Medical Device Regulatory Comparison
Compare the medical device registration pathways, classification, and regulatory requirements of TGA (Australia) vs BfArM (Germany).
TGA
Therapeutic Goods Administration (Australia)
Australia
The TGA regulates medical devices in Australia under the Therapeutic Goods Act 1989. Australia uses a risk-based classification system aligned with GHTF/IMDRF. The TGA is an MDSAP participating author…
Class I, IIa, IIb, III, AIMD
ARTG inclusion via conformity assessment
- ▸ARTG registration
- ▸Conformity assessment
- ▸MDSAP participation
- ▸Adverse event reporting
- ▸Post-market surveillance
BfArM
BfArM — Germany Medical Device Regulatory Authority
Germany
BfArM is the national regulatory authority responsible for medical device oversight in Germany. It manages device registration, market surveillance, and adverse event reporting within the Europe regul…
EU MDR classes
BfArM registration
- ▸Device registration
- ▸Market surveillance
- ▸Adverse event reporting
- ▸Import/export control
MedFlux monitors both TGA and BfArM in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.
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