Review of incidents and vigilance investigations involving medical devices From National Agency for the Safety of Medicines and Health Products (ANSM) 🇫🇷 Reference document Review of incidents and vigilance investigations of medical devices in your approach 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 July 18, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Assessment, designation and notification of conformity assessment bodies in France From National Agency for the Safety of Medicines and Health Products (ANSM) 🇫🇷 Reference document Assessment, designation and notification of conformity assessment bodies in France in your application process 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 October 7, 2022 Other (Non-Commercial) 0 reuses 0 favorites
France meeting outcome statement From International Medical Device Regulators Forum (IMDRF) 🌍 Outcome statement: France meeting outcome statement Metadata quality: Metadata quality: Data description empty Files documentation missing 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: 44.44444444444444/100 Updated on September 9, 2021 Other (Public Domain) 0 reuses 0 favorites
Commission Decision (EU) 2018/1617 of 25 October 2018 concerning a measure adopted by France pursuant to Council Directive 93/42/EEC with regard to the Terrafor and Defiligne medical devices (notified under document C(2018) 6943) (Text with EEA relevance.) From European Parliament 🇪🇺 Commission Decision (EU) 2018/1617 of 25 October 2018 regarding France's measure on Terrafor and Defiligne medical devices. 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 October 25, 2018 Creative Commons Attribution 4.0 0 reuses 0 favorites