GHTF Study Group 5 - Clinical Safety/Performance From International Medical Device Regulators Forum (IMDRF) ๐ GHTF Study Group 5 - Clinical Safety/Performance documents 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 November 2, 2012 Other (Public Domain) 0 reuses 0 favorites
Provision No. 7802/2021 From National Administration of Drugs, Food and Medical Devices (ANMAT) ๐ฆ๐ท Article 8 of ANMAT Provision No. 6052/13 is hereby amended to read as follows: "The qualification shall be granted for a term of 5 (five) years after which it shall automatically expire, and the company shall not continue performing the activities for which it was duly qualified by this Nationalโฆ 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 January 1, 2021 Creative Commons Attribution 4.0 0 reuses 0 favorites
Application of transitional provisions concerning validity of certificates issued in accordance to the directives From European Commission ๐ช๐บ This document discusses the application of transitional provisions for the validity of certificates issued by notified bodies. Metadata quality: Metadata quality: Data description filled 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: 55.55555555555556/100 Updated on September 6, 2023 Creative Commons Attribution 4.0 0 reuses 0 favorites
Use of Public Human Genetic Variant Databases to Support Clinical Validity for Genetic and Genomic-Based In Vitro Diagnostics : Guidance for Stakeholders and Food and Drug Administration Staff From Food and Drug Administration (FDA) ๐บ๐ธ This document provides guidance on using public genetic variant databases to support clinical validity for in vitro diagnostics. Metadata quality: Metadata quality: Data description filled Files documentation missing License filled Update frequency not followed File formats are closed Temporal coverage filled Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 66.66666666666666/100 Updated on April 9, 2019 Other (Public Domain) 0 reuses 0 favorites
Reporting Information Regarding Falsification of Data From Food and Drug Administration (FDA) ๐บ๐ธ Document number 2010-3123. The Food and Drug Administration (FDA) is proposing to amend its regulations to require sponsors to report information indicating that any person has, or may have, engaged in the falsification of data in the course of reporting study results, or in the course ofโฆ 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 February 19, 2010 Other (Public Domain) 0 reuses 0 favorites
Notice on the extension of the validity of the certificate of registration of medical devices for single-use infusion sets and other products From National Medical Products Administration (NMPA) ๐จ๐ณ FGWJ-2006-10081 Metadata quality: Metadata quality: Data description empty 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: 55.55555555555556/100 Updated on December 29, 2006 Other (Public Domain) 0 reuses 0 favorites