Therapeutic Goods Administration
The Therapeutic Goods Administration (TGA) has made regulatory changes to the way they will govern the production or customisation of medical devices. These changes will pertain to Occupational Therapists who make any devices that are “intended to diagnose, prevent, monitor, treat or alleviate a disease or injury."
June 2021: TGA Consultation: Refinements to regulatory changes
OTA is pleased to advise that TGA has made refinements to their proposed regulatory changes in response to feedback provided across the sector. In summary, they have proposed the following principles that should reduce unnecessary regulatory burden for occupational therapists and other Allied Health providers:
- Reduction or removal of unnecessary regulatory burden by:
- not regulating products where there is no risk to safety (a no-harm principle); or
- not regulating twice (that is, where suitable frameworks for product or system oversight are already in place).
- Applying an appropriate level of oversight that is commensurate with the risk of the device.
- Ensuring the Australian regulatory requirements for medical devices are met, thereby ensuring devices are safe and fit for their intended purpose.
The regulatory refinement also includes TGAs proposed view that:
- Where a medical device has been “prescribed” by a registered health professional and is manufactured by a qualified or accredited professional according to the specifications provided by the healthcare practitioner, risks can be adequately mitigated (e.g. Class I (low-risk) patient-matched medical devices could be exempted where they are being manufactured by a health professional registered with the Australian Health Practitioner Regulation Agency (AHPRA) under the Health Practitioner Regulation National Law Act 2009, and whose scope of practice encompasses the production of the patient-matched medical devices that they are producing).
- The devices produced are intended to be used by a patient of the healthcare facility, registered provider or AHPRA-registered health professional.
Further details of these refinements are available in the “Consultation: Proposed refinements to the regulation of personalised medical devices. OTA will be submitting a response to the TGA based on member feedback and we invite you to make independent submissions to TGA through their Consultation Hub. All submissions are due by 14 July 2021.
May 2021: TGA Webinar and FAQs
OTA is pleased to share with you the transcript of the TGA webinar and Q&A held on 10 May 2021. This interactive webinar was presented by TGA at the request of OTA, AHTA and APA to further clarify how the regulatory changes may affect allied health clinicians and to provide a platform for members to discuss issues of concern. This transcript includes answers to all the questions raised during the webinar that you may find useful to refer to.
April 2021: TGA Update: Information Webinar
In recent weeks, the OTA, AHTA and APA have collaborated with the TGA on a webinar presentation that will assist members to learn about the regulatory changes from TGA. The webinar will include:
- The background around the regulatory environment for medical devices
- An overview of the changes
- Specific examples demonstrating the impact of the new framework
- Information about the deadlines and transition periods for impacted devices
- Next steps for impacted stakeholders.
The webinar will be held on Monday 10 May 2021 at 7.00 pm – 8.00 pm AEST
Register for the webinar to find out more about how these regulatory changes may affect you.
March 2021: TGA Update: Is my product a medical device?
OTA is aware that there are many concerns about how the TGA regulatory changes will affect occupational therapy practice. We are discussing your concerns directly with TGA who will provide more detailed information soon. We will provide further information when it comes to hand.
In the meantime, we encourage you to familiarise yourself with the TGA Regulatory Changes and make use of the TGA interactive decision-making tool to help you determine if your product is a medical device and if it should be included in the Australia Register of Therapeutic Goods (ARTG).
February 2021: TGA Regulatory Changes
Many of you will be aware that the Therapeutic Goods Administration (TGA) is planning to change regulatory arrangements for those clinicians who manufacture items of assistive technology or who adapt pre-fabricated devices beyond their design envelope.
We are pleased to advise that TGA have extended the date of implementation so more consultation can take place. They will not take effect from 25 February 2021 as first proposed.
We recommend you review the proposed regulatory changes in the overview of the TGA Framework on the TGA website.
We will be consulting with the TGA about the scope of their proposed changes and how they may (or may not) affect you.
We will keep you informed of developments.