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Posted 29 May 2012 | By Ansis Helmanis
A new guidance manual for the in vitro diagnostic (IVD) business sector is intended to assist companies in how to obtain the right to market their products in Brazil. The Manual was developed by Brazil's national regulatory agency, Anvisa, in collaboration with the Brazilian Agency for Industrial Development (ABDI) and the Agency for Support to Entrepreneurship and Small Business (Sebrae).
The collaborative effort is especially intended to assist local companies to avoid the mistakes that could result in a denial of marketing approval.
Read more:
MANUAL PARA REGULARIZAÇÃO DE PRODUTOS PARA DIAGNÓSTICO DE USO IN VITRO NA ANVISA
More Breaking News from RegLink
Tags: Small Business, brazil, IVD, guidance, medical device
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