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Medical devices regulation: an introduction
This information is provided to assist you if you are new to engaging with the TGA and Australia's regulatory framework for medical devices. It will introduce you to some of the concepts and terminology used in medical device regulation.
Do not rely on this information for any regulatory purpose, including applying to enter a medical device on the Australian Register of Therapeutic Goods (ARTG).
Our risk-based approach to regulating therapeutic goods is designed to ensure that the level of regulation matches the risks posed by particular therapeutic goods.
Medical devices including in vitro diagnostic (IVD) devices are assessed against the Essential Principles and in line with their intended purpose and risk-based classification. The regulatory framework for medical devices spans the life of the device and includes:
- pre-market assessment: conformity assessment
- market authorisation: inclusion in the ARTG
- post-market monitoring: continuing compliance with all regulatory, safety and performance requirements and standards.
Supplying medical devices
Medical devices must be entered on the ARTG before they can be lawfully:
- supplied in Australia
- imported into Australia
- exported from Australia.
A person or company who is legally responsible for supplying a device in Australia is called a sponsor.
What is a medical device?
Medical devices are defined by section 41BD of the Therapeutic Goods Act 1989 (the Act). You should refer to this definition for any regulatory purpose, including preparing your application.
In summary, medical devices:
- are used for humans
- are intended to provide therapeutic benefits, or modify or monitor anatomy or physiological functions of the body
- generally achieve their purpose by a physical, mechanical or chemical action.
For example, implantable prostheses are medical devices due to their function to replace and/or modify the human anatomy and/or a physiological process.
In vitro diagnostic (IVD) devices) are also regulated in Australia as a subset of medical devices.
What is an IVD medical device?
In vitro diagnostic (IVD) medical devices are defined in the Therapeutic Goods (Medical Devices) Regulations 2002 (the MD Regulations). You should refer to this definition for any regulatory purpose, including preparing your application.
Typically, IVDs are pathology tests (and related instrumentation) used to carry out testing on human samples where the results are intended to assist in clinical diagnosis or in making decisions concerning clinical management.
Kind of device
Under the Act, a 'kind of medical device' must be included in the ARTG prior to supply in Australia unless an exemption applies. For example custom-made medical devices, which are regulated under the Act, are exempt from the requirement to include them in the ARTG.
What makes a kind of medical device?
The criteria for a kind of medical device depend on its classification:
- High risk devices
- For high risk devices (Class III and AIMD, and most Class 4 IVD medical devices), a 'kind of device' is a fairly narrow grouping restricted to a single Unique Product Identifier (UPI), typically covering design variations of a single device such as devices with different length, width, shape, etc. (defined in the MD Regulations as variants).
- Lower risk devices
- For lower classifications, a 'kind of medical device' is a broader concept and covers a range of similar products which have the same sponsor, manufacturer, classification, and are described by the term of the same Global Medical Device Nomenclature (GMDN) code.
- For example, a single ARTG entry may cover a range of different models or brands of similar devices, such as the multiple variations of intravenous infusion sets from the same manufacturer and sponsor.
How it works in practice
New products which are devices of the same kind may be supplied under an appropriate existing ARTG entry without further clearance by, or notification to, the TGA (unless required under conditions of ARTG inclusion, or when information entered on the ARTG in relation to the device should be corrected).
However, any new device which fits within the 'kind' must meet the requirements of the conformity assessment procedures implemented by the manufacturer in relation to that kind of device (and in line with the risk of the device will be assessed or monitored via ongoing certification by either TGA or a European notified body).
Classification of medical devices
The intended purpose and the risk management approach underpin the classification system for medical devices, and it's the manufacturer who is responsible for classifying their medical device(s).
The higher the classification level of a device, the higher the requirements for the conformity assessment procedures that manufacturers must apply to their device.
Multiple classification rules may apply for any given medical device. The device will be classified at the highest applicable classification.
The classification rules for medical devices are prescribed in Schedule 2 and Schedule 2A of the MD Regulations and outlined in the ARGMD.
Classification of medical devices (not IVD medical devices)
Medical devices, other than IVD medical devices, are classified with regard to their intended purpose. In particular, the classification rules take into account the degree of invasiveness in the human body, the duration and location of use, and whether the device relies on a source of energy other than the body or gravity.
Examples of devices with different classifications are summarised in the following table.
|Class I||Low||Surgical retractors, tongue depressors|
Class I – supplied sterile
Class I – incorporating a measuring function
|Low-medium||Hypodermic needles, suction unit|
|Class IIb||Medium-high||Lung ventilator, surgical meshes|
|Class III||High||Heart valves, devices containing medicines or tissues, cells or substances of animal, biological or microbiological origin|
|AIMD (Active Implantable Medical Devices)||High||Implantable defibrillator|
More information on the classification of medical devices (not IVD medical devices) can be found in Schedule 2 of the MD Regulations. You can also refer to Section 4 of the ARGMD.
Classification of IVD medical devices
The classification of IVD medical devices is based on their intended purpose and the public health risk or personal risk that may arise from an incorrect result.
The higher the potential risk an incorrect result would pose, the higher the classification.
Examples of IVD medical devices with different classifications are summarised in the following table.
|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||
More information about the classification of IVD medical devices can be found in Schedule 2A of the MD Regulations and Classification of IVD medical devices.
The Essential Principles set out the fundamental design and manufacturing requirements for medical devices.
Medical devices must comply with the Essential Principles, and the manufacturer must apply appropriate conformity assessment procedures to ensure compliance of their devices with the Essential Principles.
Among other things, before a medical device can be supplied in Australia, the sponsor must ensure (and be able to demonstrate) that the device meets all applicable Essential Principles so it is safe and performs as intended.
There are six general Essential Principles that apply to all devices (relating to health and safety, including long-term safety, with benefits outweighing the risks), and a further nine Essential Principles about design and construction that apply to devices on a case-by-case basis.
This principles-based regulatory framework caters for technological advances and changes in the development of new medical devices and provides flexibility for manufacturers. It does not mandate the means by which a manufacturer must prove that they have met the Essential Principles.
More information on the Essential Principles can be found in Schedule 1 of the MD Regulations and Section 3 of the ARGMD.
Pre-market assessment: conformity assessment of medical devices
Conformity assessment is the systematic and ongoing examination by the manufacturer of evidence and procedures to determine that the safety of a medical device is acceptable and the device performs as intended and, therefore, conforms to the Essential Principles.
The applicant must be able to demonstrate that the appropriate conformity assessment procedure has been applied to their device in order to apply for inclusion of the medical device in the ARTG.
This should be demonstrated by providing appropriate certification issued to the manufacturer by an appropriate assessment body (e.g. the TGA or a European notified body).
The level of conformity assessment required must match the level and nature of the risks associated with the use of the device, ranging from manufacturer self-assessment for low risk devices through to an assessment of the manufacturer's quality management system and examination of the design of the specific device by a conformity assessment body for the highest risk devices.
What type of conformity assessment certification does the manufacturer need?
Specific high risk medical devices
Manufacturers must hold a conformity assessment certificate issued by the TGA in relation to medical devices that contain medicines or tissues, cells or substances of animal, biological or microbiological origin; or if it is a Class 4 IVD medical device.
Other medical devices
For other medical devices, and given the close parallels between the European and Australian regulatory frameworks, the TGA generally accepts conformity assessment certification (EC Certificates) from European notified bodies issued under the European Medical Device Directives.
More information about conformity assessment can be found in Section 5 of the ARGMD.
Market authorisation: inclusion of medical devices in the ARTG
Auto-inclusion of medical devices in the ARTG
Class I medical devices (not-IVD medical devices) that do not have measuring function and are not intended to be supplied sterile, and some Class 1 IVD medical devices that are not intended to be used for self-testing or point-of care, or to be supplied for use under the pharmaceutical benefits scheme or in national screening program, can be 'auto-included' in the ARTG. Sponsors of these devices must fill in and submit an electronic application (Medical Device Application) to the TGA; however they are not required to submit any other documents to the TGA at the time of ARTG inclusion.
The sponsors of such devices, however, must have a copy of the manufacturer's declaration of conformity for the device and be able to provide it to the TGA on request together with the other documentation relevant to the device (e.g. labelling, instruction for use, advertising material, and evidence of the performance of the device).
For any other device, before an application to include the medical device in the ARTG can be made, the applicant should submit a copy of the conformity assessment certification issued to the manufacturer by an appropriate conformity assessment body or a declaration of conformity made by the manufacturer (if relevant).
This document should be submitted to (and accepted by) the TGA as Manufacturer's Evidence before an application for inclusion of the device in the ARTG can be made.
Sponsors should be in Australia, and are usually an Australian importer of overseas manufactured medical devices. Applicants must have a relationship with the manufacturer to enable them to fulfil their regulatory obligations, including obtaining information requested by the TGA from the manufacturer.
TGA assessment of applications for ARTG inclusion
The degree of rigour of the TGA's assessment of applications for inclusion of medical devices in the ARTG depends on the intended purpose and risk classification of the device, and the source of the conformity assessment certification.
The TGA may approve the inclusion of a device in the ARTG based on the information provided in the application received, or TGA may select an application for audit assessment. The audit of the application may involve a desktop review of information such as the labelling, instructions for use, technical and advertising materials for the device, clinical evidence, risk management documentation for the device, reports from the notified bodies, or microbiology assessment.
The scope of any audit will depend largely on the issues identified by the TGA as requiring further scrutiny.
Applications for devices, such as Class III, AIMDs and selected Class IIb medical devices, must be selected for audit (mandatory application audits) where the manufacturer's conformity assessment certification was issued by a European notified body.
Applications for certain IVD medical devices (e.g. those intended for self-testing or use at the point of care; or applications for Class III IVD medical devices supported only by an ISO 13485 certificate) must also be selected for audit.
Post-market assessment of medical devices
Maintenance of conformity assessment
Once a device is approved, manufacturers are expected to continue to monitor the performance and safety of their devices and ensure continued compliance with the Essential Principles. This surveillance program is part of the quality management system aspect of their conformity assessment, and will be periodically checked by the certifying body (whether this is the TGA or a European notified body). These surveillance programs should be appropriate to the intended purpose and risks of the device.
The data generated from safety and adverse event reports and complaints, newly identified risks, literature, any updated or new clinical investigations, significant regulatory actions and formal surveillance activities such as registries should be used by the manufacturer to review the performance, safety and benefit-risk assessment of the device.
TGA post-market vigilance and monitoring
The medical device regulatory framework includes provision for post-market monitoring by the TGA, including:
- risk assessment and investigation of medical device adverse event and complaint reports
- checking evidence of conformity against the Essential Principles
- conducting periodic inspections of manufacturers' quality management systems and technical documentation
- imposing specific requirements for manufacturers and sponsors to report, within specified timeframes, adverse incidents and other information involving their medical devices.
Post-market monitoring by the TGA is carried out to ensure the ongoing regulatory compliance and safety of medical devices supplied to the Australian market.
In support of the TGA's post-market monitoring activities, the sponsor of a medical device has ongoing responsibilities once a device has been included in the ARTG. These statutory responsibilities include that the sponsor must report to the TGA:
- adverse incidents
- overseas regulatory actions
- the results of investigations undertaken by the manufacturer, such as further clinical studies and reviews of adverse events.
The sponsor must also obtain requested information from the manufacturer and maintain distribution records.
All adverse event reports or complaints received by the TGA are entered into a database, and a risk assessment undertaken by a panel of clinicians and scientists within the TGA to determine if investigation is required. Expert advice may be sought during an investigation.
The outcomes of TGA's investigations may result in:
- product recovery (recalls)
- hazard and safety alerts
- product modification/improvement by a manufacturer
- surveillance audits of manufacturing sites.
For more information on any of the sections above, please refer to the Australian Regulatory Guidelines on Medical Devices (ARGMD).