Application audit (technical file review) of IVD medical device applications From Therapeutic Goods Administration (TGA) 🇦🇺 Prepare for a technical file review as part of your application to include an in vitro medical device in the Australian Register of Therapeutic Goods. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on March 27, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Guide No. 6 version 2 of 11/01/2017 From Brazilian Health Regulatory Agency (Anvisa) 🇧🇷 Guidelines for the Technical File for the Registration of Medical Products: RDC No. 40/2015 Metadata quality: Metadata quality: Data description empty Files documented License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on January 16, 2017 Other (Public Domain) 0 reuses 0 favorites
Guide No. 6 version 1 of 15/06/2016 From Brazilian Health Regulatory Agency (Anvisa) 🇧🇷 Guidelines for the Technical File for the Registration of Medical Products: RDC No. 40/2015 Metadata quality: Metadata quality: Data description empty Files documented License filled Update frequency not followed File formats are closed Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 55.55555555555556/100 Updated on June 23, 2016 Other (Public Domain) 0 reuses 0 favorites