Presentation: Manufacturing medical devices
An introduction to the work of Australia's regulator of therapeutic goods
Presentation: Life cycle of medical devices
Microbiology data requirements for Submissions for registration of sterile products
The regulation of biologicals in Australia
Prescription medicine registration process - Industry and TGA expectations
Presentation: Advertising cosmetic injectables - Complying with the therapeutic goods legislation
What’s in a name - biosimilars?
Presentation: TGA - Software inspections and therapeutic goods
An update on risk management plans - an evaluator's perspective
Events presentations-pac-141010
Presentation: Pacemaker investigation
Advertising Medical Devices to Consumers: Complying with the legislation
Presentation: eSubmissions in Australia - Part 1
Presentation: eSubmissions in Australia - Part 2
Clinical Trials - TGA Role
Risk management plan (RMP) requirements: When and why is an RMP required
Risk management plans - an overview
ARCS Pharmacovigilance update
The regulation of complementary medicines
