Brazil’s Health Authority Publishes Guidance on Monitoring International Health Regulation (IHR) Core Capacities at Designated Points of Entry

Brazil’s Health Authority Publishes Guidance on Monitoring International Health Regulation (IHR) Core Capacities at Designated Points of Entry

Brazil’s Health Authority Publishes Guidance on Monitoring International Health Regulation (IHR) Core Capacities at Designated Points of Entry

Published: December 2025
Open for contributions until February 16, 2026

Brazil’s National Health Surveillance Agency (Anvisa) has released a new guidance document to support the monitoring and evaluation of International Health Regulation (IHR 2005) core public-health capacities at the country’s designated Points of Entry (PoE) — including airports, ports, and key border crossings.

The guidance is currently in force and open to public and institutional contributions until 16 February 2026, via email submission to:
Email: [email protected]


Strengthening Brazil’s Readiness Under the International Health Regulations

The International Health Regulations (IHR 2005) — adopted under the World Health Organization framework — require signatory countries to maintain minimum public-health surveillance and response capabilities, particularly at international Points of Entry where infectious-disease risks and health emergencies may emerge.

Anvisa’s new guidance is intended to:

  • standardize monitoring practices
  • reinforce disease-surveillance capability
  • improve preparedness for health emergencies
  • align local procedures with global WHO standards

This initiative supports prevention, rapid response, and cross-border health security, strengthening Brazil’s obligations under international health law.


What the Guidance Covers

The document provides technical orientation on:

  • evaluation of operational readiness at Points of Entry
  • core capacities for detecting and responding to public-health risks
  • incident reporting and communication procedures
  • inter-agency coordination mechanisms
  • preventive and response measures during emergencies

The guidance applies to designated international entry points responsible for health surveillance involving:

  • passenger health events
  • transport-related outbreaks
  • emergency measures at borders
  • international public-health notifications

Open Consultation — Stakeholder Participation Encouraged

In line with Brazil’s commitment to transparent regulatory governance, Anvisa has opened the guidance for public consultation.

Deadline for contributions:
16 February 2026

Email for submissions:
[email protected]

Contributions are encouraged from:

  • public-health authorities
  • airport and transport operators
  • port authorities
  • regulatory and compliance professionals
  • international-trade stakeholders
  • risk-management and emergency-response teams

Why This Matters

In a highly connected global environment, strong border-level readiness is critical to preventing:

  • cross-border disease transmission
  • economic disruption
  • public-health crises
  • travel and logistics risks

Brazil’s updated framework reflects:

  • greater awareness following the pandemic
  • regulatory maturity
  • commitment to preparedness and resilience
  • alignment with WHO safety standards

Strategic Implications for Businesses & Operators

Organizations operating in aviation, shipping, logistics, tourism, and cross-border commerce are encouraged to:

  • review internal risk-response frameworks
  • align procedures with IHR-based controls
  • strengthen crisis-response planning
  • ensure documentation readiness
  • coordinate closely with authorities supervised by Anvisa

Final Outlook

This new guidance represents an important advance in health-security governance at Brazil’s international gateways. By reinforcing International Health Regulation-based procedures at Points of Entry, Brazil enhances its capacity to prevent, detect, and respond quickly to public-health threats, supporting both public safety and economic continuity.

Stakeholders are encouraged to follow developments after the consultation period and — where relevant — participate before the 16 February 2026 deadline.

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