capas regulatory affairs - rdc 665-22

RDC 665/22

The new RDC 665 came into force in May 2022, which provides for Good Manufacturing Practices for Medical Products and In Vitro Diagnostic Products, applying to manufacturers, importers and distributors who sell in Brazil.

For you who are an entrepreneur in the health market or looking for ways to enter the sector in an organized way, within the current legislation and with all the necessary consulting support, count on our team of experts!

Para você que é empreendedor do mercado da saúde ou está buscando formas de entrar no setor de forma organizada, dentro das legislações vigentes e com todo o suporte de consultoria necessário, conte com nossa equipe de especialistas!

Contact us!

-> regulatory@enzytec.com

-> +55 31 99145-9259


Any questions? Contact us and you will be answered soon!