Registration manuals for health use materials and medical equipment undergo a review process

On 05/08/2025, the National Health Surveillance Agency (Anvisa) issued an update regarding Registration manuals for health use materials and medical equipment undergo a review process. The agency is reviewing these manuals to improve the quality of instruction processual for device registration, aiming to reduce demands and indeferimentos. The preliminary versions of the manuals were made available to various industry associations, including Abiis, Abimed, Abimo, and Abraidi, to gather contributions from key stakeholders involved in the petitioning process.