Regulatory consulting and technical support services for medical device legalization, including safety and efficacy documentation, clinical evaluation protocols, and registration guidance with ANVISA, FDA, CE marking, and international regulatory agencies.
Manufactured by
MSC MED ENGENHARIA E TECNOLOGIA MEDICA LTDA
Florianopolis, Brazil
MSC MED combines scientific expertise with extensive knowledge of the Brazilian, American and European regulatory framework, offering intelligence and methodologies that assist in the development of medical device design, with a focus on ensuring safety and effectiveness to the end user. Focusing on customized customer service, we specialize in guiding companies in the dental - medical - hospital sector to overcome the technical and regulatory barriers applicable while obtaining approval for the commercialization of medical products. The company handles low, medium and high complexity processes, conducting the process partially or completely to obtain regulatory approval.
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Vera Rosas Group · Brazil
Regulatory consultancy service specializing in medical device registration, inspection, and compliance across 5 continents. Provides end-to-end support for product legalization, quality assurance, and ANVISA protocol documentation to facilitate market approval and regulatory adherence.
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.
Vera Rosas Group · Brazil
Regulatory affairs and product registration services for medical devices and IVDs, including ANVISA submissions, compliance documentation, company legalization, and quality assurance across multiple jurisdictions and continents.
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