The TGA thanks respondents who provided a submission in response to the public consultation paper, Regulation of software, including Software as a Medical Device (SaMD) .
This consultation was related to the implementation of the Australian Government Response to the Review of Medicines...
Section 19A database has been updated to include new approvals
New webinar on GMP application pitfalls
Learn about Cyber Security for your Medical Device
Last month's news & updates
The Therapeutic Goods Administration is part of the Health Products Regulation Group