Philippines to adopt ASEAN medtech registration requirements: have your say
This article was originally published in Clinica
Executive Summary
The Philippines Food and Drug Administration is inviting feedback from stakeholders on its proposal to adopt new documentary requirements for the registration of medical devices based on the ASEAN Medical Device Directive. The proposed requirements will not apply to in vitro diagnostics and refurbished medical devices as the FDA intends to issue separate requirements for these products at a later date.