Australian ARTG Listing
ComplianceAcuity has resident Consultants abroad in order to ensure legitimate continuity with far-away regulatory markets like Australia. This ensures that each project has the benefits of essential local insights and resources.
- ComplianceAcuity has simplified the maze of TGA (Therapeutic Goods Administration) requirements associated with entering a medical device on the Australian Register of Therapeutic Goods (ARTG).
- ComplianceAcuity has organic “hands-on” experience successfully meeting TGA premarket requirements for a broad range of therapeutic products including, but not limited to, sterile implantable medical devices, software-based devices, active devices, and Over-the-Counter (OTC) medicines.
Testimonials
“Kevin has the knowledge and experience to provide excellent regulatory guidance. Kevin has also provided regulatory guidance regarding import to foreign countries…His knowledge and attention to detail exceeded my expectations. I look forward to working with Kevin on future projects.”
- QA Manager, Class II and III Devices