Implementation of medical devices future regime From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ A roadmap outlining the intended timelines for delivering a future regulatory framework for medical devices and an intended policy on international recognition. 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 3, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Normative Instruction - IN nΒΊ 283 of 07/03/2024 From Brazilian Health Regulatory Agency (Anvisa) π§π· Approves the list of Technical Standards for the certification of conformity of equipment under the Health Surveillance regime Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on March 8, 2024 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 830 of 06/12/2023 From Brazilian Health Regulatory Agency (Anvisa) π§π· Provides for risk classification, notification and registration regimes, labeling requirements and instructions for use for in vitro diagnostic medical devices, including their instruments. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on December 11, 2023 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 825 of 26/10/2023 From Brazilian Health Regulatory Agency (Anvisa) π§π· Establishes the minimum identity and quality requirements for surgical gloves and gloves for non-surgical procedures made of natural rubber, synthetic rubber, a mixture of natural and synthetic rubbers and polyvinyl chloride, under the health surveillance regime. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on October 30, 2023 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 810 of 17/08/2023 From Brazilian Health Regulatory Agency (Anvisa) π§π· Amends Collegiate Board Resolution - RDC No. 751, of September 15, 2022, which provides for risk classification, notification and registration regimes, and labeling requirements and instructions for use of medical devices. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on August 18, 2023 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 777 of 01/03/2023 From Brazilian Health Regulatory Agency (Anvisa) π§π· Amends Collegiate Board Resolution - RDC No. 751, of September 15, 2022, which provides for risk classification, notification and registration regimes, and labeling requirements and instructions for use of medical devices. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on March 2, 2023 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 751 of 15/09/2022 From Brazilian Health Regulatory Agency (Anvisa) π§π· Provides for risk classification, notification and registration regimes, labeling requirements and instructions for use of medical devices. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on September 21, 2022 Other (Public Domain) 0 reuses 0 favorites
Collegiate Board Resolution - RDC No. 423 of 16/09/2020 From Brazilian Health Regulatory Agency (Anvisa) π§π· Amends Collegiate Board Resolution - RDC No. 27, of June 21, 2011, Collegiate Board Resolution - RDC No. 36, of August 26, 2015, and Collegiate Board Resolution - RDC No. 40, of August 26, 2015, to provide for the extinction of the registration regime and the migration of risk class II medicalβ¦ Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on September 18, 2020 Other (Public Domain) 0 reuses 0 favorites
Normative Instruction - IN no. 3 of 26/08/2015 From Brazilian Health Regulatory Agency (Anvisa) π§π· Regulates item I of art. 20 of Resolution of the Collegiate Board of Directors-RDC no. 36, of August 26, 2015, which provides for risk classification, registration and registration control regimes and labeling requirements and instructions for use of in vitro diagnostic products, including theirβ¦ Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on August 26, 2015 Other (Public Domain) 0 reuses 0 favorites
Provision No. 194/99 From National Administration of Drugs, Food and Medical Devices (ANMAT) π¦π· Inspection Regime for Manufacturers or Importers of Medical Products - BO 10/27/99 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 January 1, 1999 Creative Commons Attribution 4.0 0 reuses 0 favorites
Provision No. 969/97 (as amended by ANMAT Provision No. 6550/2008). From National Administration of Drugs, Food and Medical Devices (ANMAT) π¦π· The Regime applicable to the clinical studies of Medical Technology, which is included as Annex I of this Provision and is an integral part of the same, is hereby approved. 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 January 1, 1997 Creative Commons Attribution 4.0 0 reuses 0 favorites