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About
Why KD&A ?
Frequently Asked Questions
Services
Medical Device Regulatory Strategy
ISO 13485/MDSAP QMS Development and Support
Technical File Documentation
Global Medical Device Registrations including ARTG Inclusions/TGA Registrations
Post-Market Surveillance
TGA Conformity Assessment/CE Marking
Promotional Materials Review
Australian TGA Sponsor
Medical Device and IVD Device Classification Assessment
Software as a Medical Device (SaMD)
Clients
Australian Sponsors/Distributors
List Your Medical Device for Sale on The Australian Market | KD&A
Medical Device Manufacturers
International Medical Device Manufacturers
Testimonials
News
Partners
Partners
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