Federal Official Gazette
SUMMONS NOTICE
The National Supplementary Health Agency – ANS, through its Directorate of Standards and Qualification of Operators – DIOPE, summons the health plan users of CENTRAL OPERADORA DE PLANOS DE SAÚDE NORTE-NORDESTE LTDA, ANS Registration No. 41.709-2, registered in the National Register of Legal Entities – CNPJ under No. 10.540.020/0001-09, who have premiums (monthly fees) due within the last 60 days, to submit copies of their proof of payment, and further requests: 1. that creditors submit copies of invoices, bills or other documents proving any credits; 3. that other interested parties provide any information they deem appropriate. The information and/or documents must be sent to the General Management for Special Monitoring and Resolution Regimes – GGAER/DIOPE/ANS through the ANS website (www.gov.br/ans) at ANSDigital – external users – electronic filing, within 07 (seven) days.
ANS news
ANS publishes Regulatory Agenda for the 2026-2028 period
The National Supplementary Health Agency (ANS) has defined the Regulatory Agenda for the 2026-2028 three-year period, establishing the priority topics to be addressed during the period. The centrality of regulation on the health plan beneficiary is the strategic guideline of the Agenda, which took into account the need to strengthen initiatives related to timely access to health services, the quality of the care provided, the coordination of care and the balance of care-related and economic relationships in the sector.
The topics are divided into three sections:
- Regulatory Topics: these are the topics for which ANS plans to implement regulatory measures during the term of the Agenda. It is important to note that there is no obligation that all regulatory topics contained in the Regulatory Agenda be concluded, during its term, with the publication of a normative act.
- Regulatory Outcome Assessment (ARR) Agenda: this is a set of regulatory outcome assessments (ARRs) that the Agency intends to carry out during the term of the Agenda. The ARR consists of verifying the effects resulting from the issuance of a normative act, considering the achievement of the objectives originally intended and the other impacts observed on the market and society as a result of its implementation.
- Development of preliminary studies: in this section, the Agency presents topics that will be studied during the term of the Agenda. Although they are not yet mature enough for a Regulatory Impact Assessment (AIR) to be prepared, ANS proposes to explore the topic in greater depth and provide transparency on the results.
Open public consultations
No updates.
Scheduled public hearings
There are no scheduled public hearings.
Open public calls for input
There is no open public call for input.
Open public calls
Discount cards, prepaid cards, or related services. Deadline: From Jun 2, 2026 to Aug 3, 2026.
Other news
ANS discusses new health plan price adjustment of up to 20%
Source: metropoles.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.