Acting on your behalf to register your medical device; communicating with the Therapeutic Goods Administration (TGA) and carrying out obligations placed on the Australian sponsor in relation to medical device or IVD device registrations, in order to meet and show compliance with the Australian Therapeutic Goods requirements.

The Australian sponsor’s details must appear on product labelling or packaging. ACRA regulatory services understand the Australian medical device and IVD market and confidently represent you and manage and maintain your registrations. Contact us to discuss.

Phone +61 400 284 808 (0400 284 808 within Australia).

Request a proposal, a quote, or send us an enquiry about how we can represent your company as your Australian sponsor.