Authorization for the import and export of human blood and its products for the manufacture of in vitro diagnostic medical devices From Ministry of Health (Italy) (MDS) 🇮🇹 Medical devices - Online forms and services 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 June 21, 2024 Creative Commons Attribution 3.0 0 reuses 0 favorites
Australian code of good manufacturing practice for human blood and blood components, human tissues and human cellular therapy products From Therapeutic Goods Administration (TGA) 🇦🇺 The Australian Code of Good Manufacturing Practice (GMP) for Blood and Blood Components, Human Tissues and Human Cellular Therapy Products (the Code) applies to Blood, Human Tissues and Human Cellular Therapy Products manufacturers that undertake the collection, processing, testing, storage,… 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 December 21, 2023 Other (Non-Commercial) 0 reuses 0 favorites
Import and export of human blood and its products for the production of in vitro diagnostic medical devices From Ministry of Health (Italy) (MDS) 🇮🇹 Medical devices - Import and export of human blood and its products for the production of in vitro diagnostic 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 January 13, 2023 Creative Commons Attribution 3.0 0 reuses 0 favorites
Consultation procedure for ancillary medicinal substances in medical devices From European Medicines Agency (EMA) 🇪🇺 Guidelines for consultation process on ancillary medicinal substances in medical devices. 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 July 31, 2023 Other (Public Domain) 0 reuses 0 favorites
Requirements for Human Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use From Food and Drug Administration (FDA) 🇺🇸 Document number E7-21565. The Food and Drug Administration (FDA) proposes to revise and update the regulations applicable to blood and blood components, including Source Plasma and Source Leukocytes, to add donor requirements that are consistent with current practices in the blood industry, and to… 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 November 8, 2007 Other (Public Domain) 0 reuses 0 favorites
Notice of Transmittal of Revision Sheet No. 1 to the National Standard for Bagged Plastic Containers for Human Blood and Blood Components, Part 1: Traditional Blood Bags From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2007-10068 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 August 3, 2007 Other (Public Domain) 0 reuses 0 favorites
Proposal for a Directive of the European Parliament and of the Council amending Council Directive 93/42/EEC, as amended by Directive 2000/70/EC, as regards medical devices incorporating stable derivates of human blood or human plasma From European Parliament 🇪🇺 This document is a proposal to amend the existing directive on medical devices to include those incorporating stable derivates of human blood or plasma. 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 August 22, 2001 Creative Commons Attribution 4.0 0 reuses 0 favorites
Resolution - RES No. 9 of 21/10/1999 From Brazilian Health Regulatory Agency (Anvisa) 🇧🇷 To approve the "Technical Regulation for Good Manufacturing Practices (GMP) of Blood Bags" and Annexes, containing technical standards and conditions necessary to guarantee the quality of plastic bags for the collection and packaging of human blood and its components. 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 21, 1999 Other (Public Domain) 0 reuses 0 favorites