Consultation on Medical Device Regulations
MDA provides consultation services for industry regarding medical device regulatory requirements and compliance matters. Stakeholders may access consultation services through the designated consultation portal.
The mda is inviting written submissions from manufacturers, sponsors, importers, and other industry stakeholders. Review the draft guidance or proposal at the official source, prepare comments identifying any practical impacts on your operations or products, and submit. Active participation helps ensure the final guidance reflects industry realities and gives your organisation early visibility of upcoming requirements.
View official source ↗