by Innovit Corporate Affairs | Sep 25, 2022 | Blog, Michelle Laurion, UDI
Brazil’s medical device market regulator, ANVISA announced major updates to its Resolution of the Collegiate Board of Directors (RDC) 185/2001. The changes will serve to strengthen the country’s medical device registration regulations upon their effective date of...
by Innovit Corporate Affairs | Sep 19, 2022 | Blog, Michelle Laurion, UDI
Australia is establishing a unique identification system for medical devices and its regulator, the Therapeutic Goods Administration (TGA) issued several updates regarding Unique Device Identification (UDI) regulations, Essential Principles for compliance requirements...
