Gasparini, Barbosa e Freire Advogados provides a legal foundation for the development of business activities involving pharmaceutical products, raw materials, cosmetics, and health-related goods—an economic sector highly subject to regulatory oversight. The Firm offers legal and regulatory counsel related to regulatory acts issued by government agencies, conducts legal analyses, and performs due diligence on manufacturers, distributors, importers, exporters, carriers, packers, pharmaceutical industries, drugstores, and pharmacies, among others.
The Firm provides advisory services on regulatory aspects, including Good Manufacturing Practices (GMP) Certification, Product Registration, Authorization, and Licensing. The legal support also encompasses the drafting, review, and negotiation of administrative contracts with the Ministry of Health (MS), the Brazilian Health Regulatory Agency (ANVISA), and other government departments and agencies. Additionally, the Firm provides legal representation in administrative proceedings before ANVISA, local health agencies, municipal governments, and other regulatory bodies.
