In Vitro Device (IVD) registration in Australia
The Australian TGA regulates IVDs as a subset of medical devices, using a risk-based approach. Their regulatory framework aligns with the recommendations of the old Global Harmonisation Task Force (GHTF), or the new IMDRF. This means that if you successfully register an IVD with the TGA then you are likely to achieve registration in other countries that align their regulations with the IMDRF. Read more about the change from GHTF to IMDRF.
Current IMDRF members Jan 2016 –
The current members are:
- Australia
- Brazil
- Canada
- China
- Europe
- Japan
- Russia, and
- the United States of America.
IVD Classification
IVDs are classified by the TGA as follows:
| Classification | Level of risk |
|---|---|
| Class 1 IVD | no public health risk or low personal risk |
| Class 2 IVD | low public health risk or moderate personal risk |
| Class 3 IVD | moderate public health risk or high personal risk |
| Class 4 IVD | high public health risk |
The same classification rules apply to both commercial IVDs and in-house IVDs.
Product Registration Services
PharmOut offers product registration services for companies wishing to register IVDs with the Australian TGA, for sale within Australia.We can provide advice on product development, preclinical and clinical research, regulatory affairs and quality assurance.
Our regulatory affairs consultants can advise on:
- CE marking of IVDs
- IVD product classification – which classification does it fall into?
- Preparation of technical files
- Risk assessments
- Quality audits
R&D Programs for Novel Products
PharmOut can assist with planning R&D programmes for novel products; designing suitable studies to meet regulatory requirements and achieving timely approvals in target countries.
Our auditors can undertake cGMP, QSR, ISO 9000, ISO 13485 audits of companies, their suppliers and subcontractors, ensuring that appropriate standards of quality are met.
CE Marking of IVDs
IVD registration in the European Union is now harmonised and products bearing the CE mark can be freely marketed in all member states.
CE marking is an important step in getting your IVD product ready to market. First you must determine which category your product falls into – you can then determine which legislation applies, and what the best route to market will be.
Our team can advise on regulatory, scientific and quality matters, including ISO 13485, FDA QSR 820 and related standards.
More Information
If you would like a quote or would need to ask questions, please contact us.