Planned maintenance may cause outages to the Department of Health and Aged Care’s network from 5:15 pm AEDT on 30 November to 10:00 pm AEDT on 1 December 2024. Access to TGA databases such as TBS Portal, ARTG and DAEN may be affected. We apologise for any inconvenience.
Role of the Therapeutic Goods Committee in the TGA's regulatory decision making process
The Therapeutic Goods Committee (TGC) is a statutory advisory committee established by the Therapeutic Goods Regulations 1990.
The TGA currently has ten statutory advisory committees from which it can obtain independent expert advice on specific scientific and technical matters to aid the TGA's regulatory decision making and other regulatory processes. The Therapeutic Goods Committee provides advice to the TGA on, amongst other things, matters relating to:
- the adoption of standards for therapeutic goods
- the requirements for labelling and packaging of therapeutic goods
- standards for the manufacture of therapeutic goods
- matters relating to medical device standards, conformity assessment standards and standards for biologicals.
The advice provided by the Therapeutic Goods Committee is an important element in the undertaking of the regulatory functions of the TGA. However, it forms only part of the information that is available to, for instance, a TGA delegate making a regulatory decision under the Therapeutic Goods Act 1989. While appropriate consideration will be given to such advice, it is important to note that neither the TGA nor a TGA delegate is obliged to follow it.
It should also be noted that information about advice provided by the committees may not become publicly available for some time after a committee has provided that advice. The purpose of this Meeting Statement is to describe in general terms the matters considered by the committee at each meeting and make this available as soon as reasonably practical after the relevant meeting.
Overview of the standards referred for advice
At the 41st meeting, the committee's advice was sought in relation to the draft Therapeutic Goods Order No. 79 General Requirements for the Labelling of Medicines, including possible amendments and proposed further consultation.
The committee's advice has now been provided to the TGA for consideration as part of the TGA's regulatory decision making process.
Other matters considered
At this meeting, the committee was provided with an update in relation to a proposal for the harmonisation of ingredient names.
Further information
Meeting statements are made publicly available after each meeting.
For further information on the Therapeutic Goods Committee, please visit TGC or contact the TGC Secretary by phone on 02 6232 8623 or email: TGC@tga.gov.au