Medical Device Registration in Australia

 

Medical Device Registration in Australia Process: 

Therapeutic Goods Administration (TGA) oversees regulation of medical devices in Australia through Australian Regulatory Guidelines for Medical Devices (ARGMD) and these guidelines closely resemble with the regulations put into place by the European Union. To gain access to the Australian market, medical device and IVD manufacturers need to include their products in the Australian Register of Therapeutic Goods (ARTG). Medical devices are obliged to be entered in the Australian Register of Therapeutic Goods (ARTG) before they can be lawfully supplied in Australia, imported into Australia or exported from Australia. currently TGA recognises CE marking, means companies who have already acquired the European market can easily meet TGA requirement. 

Classification of Medical Devices in Australia  

In Australia, medical devices are classified as per the Australian Therapeutic Goods (Medical Devices) Regulations 2002. Medical devices are classified with respect to their intended purpose. Particularly, the classification rules take into consideration the degree of invasiveness in the human body, the duration use, location of use, and whether the device relies on a source of energy other than the body or gravity.   

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Contact details –

Phone  no -  93702 83428

Mail id – enquiry@operonstrategist.com

If  You Want Medical Devices Services Consultation For Following.

1. Medical Device Consulting 
2. cdsco registration 
3. FDA 510k Clearance 
4. ce mark medical device 
5. CDSCO Manufacturing License 
6. CDSCO import license 
7. TURNKEY PROJECT CONSULTANT 
8. medical device manufacturing 
9. iso 15378 certification 
10. 21 cfr part 210 and 211 
11. ISO 13485 Medical Device Consultant 
12. Primary Packaging Turnkey Project Consultant 
13. Clean Room Design Consultant 
14. manufacturing site conceptualization 
15. Market Analysis and feasibility for Medical Devices 
16. manufacturing plant layout design 
17. medical device design and development 
18. DMF file submission guideline 
19. 21 cfr part 820 
20. qms certification services 
21. capa management 
22. design control requirements 
23. medical device process validation 
24. combination product 
25. continuous improvement program 
26. Medical Device Compliance & Regulatory Services 
27. Cdsco India authorized agent for medical device