MedDream Expands into Australia with TGA Class IIb Registration

We’re proud to announce another important global milestone: MedDream DICOM Viewer is now officially registered with the Therapeutic Goods Administration (TGA) in Australia as a Class IIb medical device.

The Therapeutic Goods Administration – Australia’s regulatory authority for therapeutic goods such as medicines, medical devices, and diagnostic tests (TGA) has registered the medical software MedDream as IIb class Radiology picture archiving and communication system application software.

This registration enables MedDream to be legally marketed and used in Australia, further strengthening our presence in the Asia–Pacific region. Together with existing registrations in Singapore, Malaysia, and Thailand, MedDream continues to expand across the eastern markets, supporting healthcare providers, OEMs, and software vendors with a trusted, vendor-neutral imaging solution.

MedDream delivers a web-based, cost-effective, customizable, and ready-to-integrate DICOM viewer, designed for seamless interoperability with PACS, VNA, EHR, EMR, HIS, RIS, eHealth platforms, patient portals, telemedicine solutions, and cloud infrastructures. MedDream combines regulatory compliance, flexibility, and proven performance—ready for modern healthcare environments.