Vera Rosas Regulatory Affairs

Vera Rosas is the most honored and reliable Regulatory Affairs consulting company in Brazil. Globally recognized in the market for its efficiency and quality, specialized in product approval by ANVISA, company legalization and compliance to GMP requirements (GMP pre-audit, ANVISA audits monitoring, implementation and training of quality procedures).

It has a portfolio of clients located in more than 40 countries and on every continent. More than 20,000 records filed with ANVISA.

Vera Rosas Regulatory Affairs is one of the companies that belong to Vera Rosas Group, with VR Medical Importadora e Distribuidora Ltda (Brazil), BioDevices (Brazil) and VLR Regulatory Affairs (EUA).

Vision: Being the most efficient Regulatory Affairs company in the Brazilian market, always working focused on Ethics, Quality and Agility of our services.

Mission: Provide services with readiness and dynamism, with the highest level of quality while maintaining a close relationship with customers.

  • Established 1999
  • Privately held company
  • 51-200 employees

Country Focus

  • Brazil
    Location Type
    Own office in the country
    Certification
    -

Sector Focus

  • Healthcare & Medical
    Sector association
    Member
    Certification
    -
  • Pharmaceutics
    Sector association
    -
    Certification
    -

Services

  • Pharmaceutical Legislation
    Description
    We provide assistance to register pharmaceutical products at ANVISA.
    Professional association
    Member
    Certification
    -
  • Health Legislation
    Description
    Consultancy on Regulatory Affairs in Brazil, medical devices and health products
    Professional association
    Member
    Certification
    -
  • Product Registration & Certification
    Description
    Assistance on company legalization, GMP process and assembling of dossiers.
    Professional association
    Member
    Certification
    -

Memberships