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Bruno Marcelos — Escritório de Advocacia

Pauta Regulatória · Daily brief

No. 28

· covers 08 a 10/11/2025

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

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

US announces deal with makers of Mounjaro and Ozempic

Source: exame.com · read the full article

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.