Senate debates

Wednesday, 19 August 2026

Documents

Therapeutic Goods Administration; Order for the Production of Documents

3:57 pm

Photo of Maria KovacicMaria Kovacic (NSW, Liberal Party, Shadow Assistant Minister for Women) | | Hansard source

At the request of Senator Antic, I move:

That there be laid on the table by the Minister representing the Minister for Health and Ageing, by no later than midday on Tuesday, 15 September 2026, all documents relating to the current evaluation of mFLUSIVA by the Therapeutic Goods Administration (TGA), including documents in draft, interim or preliminary form and documents generated or received to date and including the following:

(a) the application dossier and all TGA evaluation reports and assessments, including drafts, preliminary, interim and first-round reports, relating to clinical, nonclinical, quality/manufacturing, statistical and pharmacovigilance matters;

(b) all documents assessing or discussing safety, efficacy and the benefit-risk profile of mFLUSIVA, including known or potential risks, safety signals, uncertainties, missing information, data gaps, Risk Management Plans (RMPs), risk-minimisation measures and proposed pharmacovigilance or post-market requirements;

(c) any post-market safety documentation, PSURs/PBRERs, signal assessments and RMP updates;

(d) all questions, requests for information or clarification, including notices pursuant to section 31 of the Therapeutic Goods Act 1989, together with sponsor responses, supplementary information and correspondence between the TGA, sponsor, evaluators or other parties concerning the evaluation of mFLUSIVA;

(e) all draft or completed Delegate's Overviews, briefing papers, internal reviews, recommendations, meeting records and expert advice, including material prepared for or received from the Advisory Committee on Medicines or other expert advisers; and

(f) all documents prepared to date concerning proposed approval, rejection, indications, conditions of registration, Product Information, RMP requirements or other regulatory outcomes, including draft recommendations, proposed decisions and any draft AusPAR or decision summary.

Photo of Katy GallagherKaty Gallagher (ACT, Australian Labor Party, Minister for the Public Service) | | Hansard source

I seek leave to make a short statement.

Photo of Sue LinesSue Lines (President) | | Hansard source

Leave is granted for one minute.

Photo of Katy GallagherKaty Gallagher (ACT, Australian Labor Party, Minister for the Public Service) | | Hansard source

The government will not be supporting this motion. We have well-established regulatory frameworks and robust mechanisms governing the development, manufacture, marketing and supply of therapeutic goods. These processes put public health front and centre whilst also balancing transparency with the need to protect commercially sensitive and confidential information. Requiring the publication of these documents would cut across that established framework and could create an adverse precedent that may discourage industry from bringing medicines to the Australian market.

Photo of Sue LinesSue Lines (President) | | Hansard source

The question is that general business notice of motion 625, standing in the name of Senator Antic, be agreed to.