Manual GQUIP_2025
ANVISA Reliance: Revolutionizing Medical Device Registration in Brazil
Contact our medical device regulation specialists and ensure your company stays updated on these regulatory advances. Our specialized team can guide you through the reliance process and maximize your success opportunities in the Brazilian market. Find out more about BPO in RA! *Budget for registration ownership transfer, Market Access Strategy, and BPO in RA services for your company: www.brisa.com.br
RESOLUTION ANVISA No. 989, OF AUGUST 15, 2025
RESOLUTION OF THE BOARD OF DIRECTORS ANVISA No. 982, OF JULY 28, 2025
SIUD User Manual
New PAC – MEDICAL DEVICES
Technical Names of In Vitro Diagnostic Medical Devices (IVD)with Multiple Risk Classification Possibilities
Ver Post