Regulatory documentation hosting and management service for ANVISA product registration in Brazil. Streamlines submission, storage, and compliance tracking of medical device and pharmaceutical registration records with Brazilian health authorities.
Manufactured by
Latini Group
Brazil
Regulatory Affairs are our expertise! | Regulatory Affairs are our expertise! Latini Group® is the consolidation of a group of reference companies with more than 30 years of experience and excellence in Regulatory Affairs, offering integrated and customized solutions for each client's needs.
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Vera Rosas Group · Brazil
Regulatory affairs and compliance service specializing in ANVISA product registration, inspection, and quality conformance. Supports medical device legalization and regulatory documentation across five continents.
QLS - QUALITY LIFE SCIENCES · Brazil
Regulatory hosting and registration service for medical devices, pharmaceuticals, and healthcare products seeking market authorization in Brazil. Manages ANVISA compliance, product registration, and notification requirements for international manufacturers entering the Brazilian market.
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Regulatory hosting and registration services for medical devices, in vitro diagnostics, pharmaceuticals, and healthcare products seeking market authorization in Brazil. Provides ANVISA-certified compliance support, documentation management, and regulatory navigation for international manufacturers.
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