The registration of medical devices is so important throughout the world that an error found in the built-in process of it can put a person’s life at stake. For every nation, its citizens are essential. They have prime importance. Government bodies cannot compromise the safety of there people. In 2002, Australia also standardized its rules towards “Registration of medical devices.” It has constructed a platform chiefly, a “regulatory body” for the assessment and classification of medical devices. That Regulatory body is called the “Australian Register of Therapeutic Goods (ARTG).” All the medical devices that are up to the mark following the prescribed rules described by ARTG are eligible for the commencement of their businesses in the medical device field in Australia. Inside ARTG, all the related companies have to register themselves. Its rules are to the point, and any loose-hand by a company can ban its product supply in the country. ARTG has some exclusions as well, which are related to low-risk consumer products.
The Process of Medical Device registration
To be able to legally supply the medical device in Australia, the person or sponsor needs to obtain two things from the manufacturer of the devices.
- The classification for the device/s
- GMDN codes for the device/s
It needs to comply with the TGA guidelines documentation
Meeting the TGA guidelines is a complex process, and all these complexities faced by the Medical device companies while registering or managing its existence on ARTG rules are handled very well by the Medical device consultancies. They have stepped in the field for that.
ALL the web of do’s and don’ts becomes the headache of these consultancies, while medical device companies can work on the core values of the business. Medical device consultants keep an eagle eye on the guidelines and don’t let it mismatch on any point. They help in regulating the business in TGA-eBusiness Services.
They are of the various kind; From design to production and from installation to servicing, they provide many services to its clients. Medical device consultants can be approached to meet the TGA guidance documentation, which is one such a thing!
Medical device management consultants hold on to all the processes of the medical device, from manufacturing to its finishing process. It gives out a strategy to meet ARTG rules throughout all development processes. The common assignments of these consultancies vary to the assessment of medical devices to Global regulatory strategy development and much more. There are some Medical device Testing consultancies too; who analyze medical device components with chemical and physical analysis
ISO Medical Device Standards
There is an ISO standard for Medical devices; ISO standard 13485, which is a proper quality control standard on which medical device companies have to lay upon, and it can also be managed by medical consultants.
ISO medical standards can also be used by internal and external bodies who want to conduct a medical audit. They must follow up with the guidelines provided by ISO 13485 while auditing a medical device company.
There is a certain process for registering medical devices in Australia. Companies treating medical devices as a product needs to comply with the ARTG rules. They also need to take care of ISO medical standards. Medical device companies have a choice to select “Medical device consultancies” to take care of it. Medical device consultancies are at service for different things. They keep an eye on the whole production process of the medical device, whether it’s about design or anything other, everything is going to be well settled with TGA guidelines.