EU MDR Transition web publication service From Therapeutic Goods Administration (TGA) π¦πΊ The EU MDR Transition web publication service provides notifications to providers and consumers going through low-risk changes, as part of the transition. 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 3 weeks ago Other (Non-Commercial) 0 reuses 0 favorites
Medical devices reforms: low-risk products From Therapeutic Goods Administration (TGA) π¦πΊ Improve consumer safety, reduce regulatory burden, and improve regulation knowledge with appropriate regulation of low-risk 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 1 month ago Other (Non-Commercial) 0 reuses 0 favorites
Outcomes of the Lower Risk Registered Over-the-Counter (OTC) Products Review Pilot Project From Therapeutic Goods Administration (TGA) π¦πΊ The TGA has finalised the outcomes of the Lower Risk Registered OTC Products Review Pilot Project 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 July 12, 2023 Other (Non-Commercial) 0 reuses 0 favorites
Medical devices reforms: Low risk products - Class 1 medical devices From Therapeutic Goods Administration (TGA) π¦πΊ Appropriate regulation of low risk devices improves their availability. 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 27, 2023 Other (Non-Commercial) 0 reuses 0 favorites
The future regulation of low risk products From Therapeutic Goods Administration (TGA) π¦πΊ The TGA response to the future regulation of low risk products has been released 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 April 13, 2023 Other (Non-Commercial) 0 reuses 0 favorites
Medical devices reforms: Low risk products - other therapeutic goods From Therapeutic Goods Administration (TGA) π¦πΊ Appropriate regulation of low risk devices improves their availability. 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 April 13, 2023 Other (Non-Commercial) 0 reuses 0 favorites
General Wellness: Policy for Low Risk Devices: Guidance for Industry and Food and Drug Administration Staff From Food and Drug Administration (FDA) πΊπΈ This document is a guidance for the industry and FDA staff on the policy for low-risk devices in the field of general wellness. 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 September 26, 2019 Other (Public Domain) 0 reuses 0 favorites
Unique Device Identification System From Food and Drug Administration (FDA) πΊπΈ Document number 2012-16621. The Food and Drug Administration (FDA) is proposing to establish a unique device identification system to implement the requirement added to the Federal Food, Drug, and Cosmetic Act (FD&C Act) by section 226 of the Food and Drug Administration Amendments Act of 2007β¦ 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 10, 2012 Other (Public Domain) 0 reuses 0 favorites