Home » TGA: Devicemakers Should Prepare for Adoption of New Standards
TGA: Devicemakers Should Prepare for Adoption of New Standards
Devicemakers manufacturing therapeutic products in Australia should implement a quality risk management system that is fully documented
and monitored for effectiveness by July, the Therapeutic Goods Administration (TGA) says. The recommendation is one of several included in a TGA presentation posted
on the agency website to prepare for new guidelines for good manufacturing practices.
International Medical Device Regulatory Monitor
International Medical Device Regulatory Monitor
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