Simplifying Global Compliance
FDAnews Device Daily Bulletin
Brazil Moves to Streamline GMP Certificates, International Standards
June 20, 2013
The prospect of a standardized single audit program for medical devices, currently being developed by the International Medical Device Regulators Forum, is fueling efforts by Brazil’s Anvisa to bring device good manufacturing practice regulations in line with international standards, an expert says.
International Medical Device Regulatory Monitor
Copyright ©2018. All Rights Reserved.
Design, CMS, Hosting & Web Development :: ePublishing