TGA – Use of market authorisation evidence from comparable overseas regulatory and assessment bodies for medical devices (including IVDs)

We are resharing this update from earlier in the year:

TGA – Use of market authorisation evidence from comparable overseas regulatory and assessment bodies for medical devices (including IVDs)

Use of market authorisation evidence from comparable overseas regulators and assessment bodies for medical devices (including IVDs) | Therapeutic Goods Administration (TGA)

Mentions CE to the directives and the regulation for products with NB Certification, no equivalent mention of UK Approved Body certification to UKCA.