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Bruno Marcelos — Escritório de Advocacia

Pauta Regulatória · Daily brief

No. 27

Automatically translated from the Portuguese edition, which prevails in case of discrepancy. Ler em português

No new items were published in the sources we monitor on this date. The open consultations and hearings below remain current.

Federal Official Gazette

No updates.

ANS news

No updates.

Open public consultations

  • CP 163. Its purpose is to receive input on the proposed updates to the List of Health Procedures and Events (Rol), specifically on the preliminary recommendation of non-incorporation for the technologies covered by UAT No. 171 – Inclisiran, UAT No. 175 – Lebrikizumab and UAT No. 176 – Momelotinib. Deadline: Nov 5, 2025 to Nov 24, 2025

Scheduled public hearings

  • Public Hearing No. 61, collection of input on the preliminary recommendation of non-incorporation for the following technologies:
    (i) UAT 171 – Inclisiran for the treatment of primary hypercholesterolemia or mixed dyslipidemia;
    (ii) UAT 175 – Lebrikizumab for the treatment of adult patients with severe atopic dermatitis who have failed, are intolerant to or have a contraindication to cyclosporine; and
    (iii) UAT 176 – Momelotinib for the treatment of intermediate- and high-risk myelofibrosis.

Date: November 19, 2025, from 9 a.m. to 1 p.m.

Open public calls for input

There are no open public calls for input.

Open public calls

No updates.

Other news

– No updates.

Sources: Federal Official Gazette (DOU) and the ANS website. Press items link to the original article. This brief is for information only and does not constitute legal advice.