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Get smart about Australia in 1 hour
If you are thinking about entering the Australian market for the first time, understanding the Therapeutic Goods Association (TGA) regulatory
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Medical device registration in Australia and New Zealand
Medical Device Registration in Australia & New Zealand
Thinking about selling your medical device or IVD in Australia or New Zealand? If your device already has CE Marking or approvals in other key
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TGA - Australia Therapeutic Goods Administration
The Therapeutic Goods Administration is the Australian regulatory authority for therapeutic goods such as pharmaceuticals, blood products and tissues
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Learn about basic demographic and healthcare market data on Australia
AUSTRALIA – Overview of medical device industry and healthcare stats
Below you will find basic demographic and healthcare market data on Australia, plus specific information about the medical device and healthcare
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Learn about the Australian TGA regulations which apply to medical devices
Australia TGA Medical Device Regulations
Log into RAMS to download the documents listed below along with more regulations and guidances for Australia. LOG INTO RAMS Related services for
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Bangladesh
Bangladesh medical device & IVD approval process
Related services: Certificate of Free Sale (CFS) for Medical Device Exports Certificate to Foreign Government (CFG) for medical devices Clinical
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In Depth: Brazil Medical Device Approval and Compliance
Brazil is one of the fastest growing device markets in the world. It’s now among the top 10 markets and spends as much on healthcare as the UK.
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