Therapeutic Goods Information (Information about Advisory Committee Meetings) Specification 2014 (Cth)
Therapeutic Goods Information (Information about Advisory Committee Meetings) Specification 2014
Therapeutic Goods Act 1989
I, JOHN SKERRITT, a delegate of the Minister for Health, make this Specification under subsection 61(5D) of the Therapeutic Goods Act 1989.
Dated
11th April 2014
(Signed by)
JOHN SKERRITT
Delegate of the Minister for Health
Name of Specification
This Specification is the Therapeutic Goods Information (Information about Advisory Committee Meetings) Specification 2014.
Commencement
This Specification commences on the day after it is registered.
Definitions
In this Specification:
Act means the Therapeutic Goods Act 1989.
Committee means any of the committees established under Divisions 1-1EB of Part 6 of the Regulations.
Regulations means the Therapeutic Goods Regulations 1990.
TGA means the Therapeutic Goods Administration, which is part of the Department of Health.
4 Therapeutic goods information
The kinds of therapeutic goods information mentioned in Schedule 1 are specified under subsection 61(5D) of the Act, for the purposes of subsection 61(5C) of the Act.
Schedule 1 Specified kinds of therapeutic goods information
(section 4)
The following kinds of therapeutic goods information, being information relating to a Committee:
Note: The following specified kinds of therapeutic goods information may be released by the Secretary to the public under subsection 61(5C) of the Act.
Information about the nature or content of any discussion about matters or items considered by the Committee at a Committee meeting, or that summarises that discussion.
Note
1. All legislative instruments and compilations are registered on the Federal Register of Legislative Instruments kept under the Legislative Instruments Act 2003. See
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