Australia’s Therapeutic Goods Administration (TGA) is now requiring sponsors of medical devices to respond directly to the agency’s postmarket product notifications using an online postmarket compliance “dashboard.”

The TGA said the secure dashboard will store information in a central location so devicemakers will not need to send information to different teams at the agency.

The agency has posted a compliance guide on its website with step-by-step instructions on how to use the new dashboard. Read the compliance guide here: bit.ly/3eYNNb0.