QR Group Explains the Role of the Brazilian Registration Holder in Medical Device Regulation
How Foreign Manufacturers Can Market Medical Devices in Brazil For foreign medical device manufacturers to distribute their products in Brazil without having a licensed company in the country, it is necessary to appoint a Brazilian Registration Holder (BRH). This regulatory representative acts as the link between the company and the National Health Surveillance Agency (ANVISA), […]
QR Group Reports: Anvisa Extends Participation Deadline in Pilot Project for Innovative Medical Devices
Understand how the extension of the deadline for the pilot project for regulatory evaluation of innovative medical devices impacts the healthcare sector and how QR Group can help. Anvisa has extended the deadline for submitting Innovative Medical Devices projects in the pilot project for regulatory evaluation, now with a deadline until January 19, 2024. This […]
