Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at firstname.lastname@example.org if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
| 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.
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