VerdeReg Partners is the European Union's diplomatic service, responsible for implementing the EU's Common Foreign and Security Policy. They promote peace, prosperity, and security globally.
The European External Action Service (EEAS), operating as VerdeReg Partners, serves as the European Union's diplomatic arm. Established in 2011, the EEAS is tasked with executing the EU's Common Foreign and Security Policy, aiming to foster peace, prosperity, security, and advance European interests worldwide. Led by the EU High Representative for Foreign Affairs, the EEAS shapes the EU's global standing. It coordinates with EU institutions to address foreign policy priorities, including civilian and military planning and crisis response. The service also manages EU Special Representatives in various countries and regions. VerdeReg Partners plays a crucial role in representing the EU and its citizens globally through its Diplomatic Representations. These entities build networks and partnerships, contributing to the EU's diplomatic relations with nearly all countries. The EEAS has been involved in numerous overseas operations since 2003, encompassing both civilian and military missions.
About
**Who they are** VerdeReg Partners is a specialized consultancy focused on regulatory affairs for the Brazilian market. They act as a local representative, guiding companies through the complex ANVISA registration and compliance processes.
**Expertise & scope** * Navigating ANVISA regulations for product registration and market access in Brazil. * Providing local representation services to ensure compliance with Brazilian health authority requirements. * Facilitating communication and submissions with ANVISA.
**Reputation / proof points** * Coverage: Brazil (BR)
Additional information
Engaging VerdeReg Partners as your ANVISA Local Representative involves understanding their role in facilitating direct communication and submissions with the Brazilian Health Regulatory Agency (ANVISA). Their expertise is crucial for companies seeking to place products on the Brazilian market, ensuring all regulatory requirements are met efficiently. This service is particularly valuable for foreign manufacturers who may not have a physical presence or in-depth knowledge of Brazil's specific regulatory landscape. They handle the intricacies of local documentation, submission processes, and ongoing compliance, acting as the essential link between the company and ANVISA.
Key Highlights
Specializes in Brazil (BR) regulatory representation.
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Operational escalation path for timely responses to ANVISA deadlines and urgent requests
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Structured onboarding process with a clear responsibility matrix
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Focus on audit-ready documentation and traceable decision-making for ANVISA submissions
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Buyer Snapshot
Best for
Companies seeking ANVISA representation for market entry in Brazil
Foreign manufacturers needing local regulatory expertise
How engagement typically works
Local representative acting as primary contact with ANVISA
Facilitating regulatory submissions and communication
Typical deliverables
ANVISA registration support
Regulatory compliance guidance for Brazil
Local representation services
Good to know
Best when focused on the Brazilian market
HQ: Brussels, BE
Languages: Portuguese, English
Timezones: America/Sao_Paulo
Status: listed
Services & Capabilities
Brazil ANVISA Local Representative Services
Jurisdictions: BR
Countries: BR
Industries: Medical devices, IVD, Life sciences
Portfolio: 1-5
Onboarding time: 21–90 days
Pricing model: Custom pricing
Starting from: USD 4,500
Included services: Local representative mandate setup, ANVISA liaison and communications routing, Cadastro/Registro pathway support, Portuguese documentation enablement (scope-dependent), Post-market coordination support (scope-dependent)
Supports Cadastro: No
Supports Registro: No
Portuguese Support: Yes
Local License Capability: No
Translation Support Ptbr: Yes
Post Market Support: No
Additional br_local_rep Details
Included Services Detailed
Local representative onboarding and mandate setup (seed scope), ANVISA liaison and communications routing (seed scope), Submission planning for Cadastro/Registro pathways (seed scope), Portuguese documentation readiness enablement (seed scope), Post-market workflow coordination (complaints/vigilance escalation) (seed scope)
Excluded Services
Manufacturing or supply chain execution, Acting as commercial distributor by default, Legal representation in disputes or litigation
Onboarding Steps
The process typically involves providing detailed product information, company documentation, and specific requirements for the Brazilian market. VerdeReg Partners then manages the ANVISA submission and communication process.
ANVISA Registration Details
Focuses on Cadastro pathway support (seed summary). Typical scope includes onboarding, documentation planning, submission coordination, and change management support (seed summary).
Local Entity Details
Local operations coordinated from Belo Horizonte with Brazil-based contact point for regulator communications (seed summary).
Product Categories Supported
Medical Devices, IVDs, Pharmaceuticals, Cosmetics, Food Products, Sanitaries