Legal supply of COVID-19 test kits From Therapeutic Goods Administration (TGA) π¦πΊ Updated information about the legal supply of COVID-19 test kits 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 16, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Legal framework From Therapeutic Goods Administration (TGA) π¦πΊ Information on advertising legislation and how we manage advertising compliance. 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 Other (Non-Commercial) 0 reuses 0 favorites
COVID-19 test kits included in the ARTG for legal supply in Australia From Therapeutic Goods Administration (TGA) π¦πΊ View COVID-19 tests approved for inclusion in the Australian Register of Therapeutic Goods (ARTG). 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 May 20, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Enforcement Rule of the Medical Devices Act From Ministry of Food and Drug Safety (MFDS) π°π· ENFORCEMENT RULE OF THE MEDICAL DEVICES ACT_Ordinance of the Prime Minister No.1819_20220721 μλ£κΈ°κΈ°λ² μνκ·μΉ(2022.7.21.) Note: MFDS offers the English version as a service to an international audience. Any discrepancies or differences created in the translation are not binding and have no legal effec... 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 March 19, 2024 Other (Public Domain) 0 reuses 0 favorites
Enforcement Rule of the Act on In-Vitro Diagnostic Medical Devices From Ministry of Food and Drug Safety (MFDS) π°π· ENFORCEMENT RULE OF THE ACT ON IN VITRO DIAGNOSTIC MEDICAL DEVICES(20201231) 체μΈμ§λ¨μλ£κΈ°κΈ°λ² μνκ·μΉ(20201231) Note: MFDS offers the English version as a service to an international audience. Any discrepancies or differences created in the translation are not binding and have no legal effect for complian... 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 March 8, 2024 Other (Public Domain) 0 reuses 0 favorites
Import From Therapeutic Goods Administration (TGA) π¦πΊ Information on the legal requirements for importing therapeutic goods into Australia, including 'unapproved' therapeutic goods and controlled substances. 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 25, 2023 Other (Non-Commercial) 0 reuses 0 favorites
Export From Therapeutic Goods Administration (TGA) π¦πΊ Information on the legal requirements for exporting medicines, medical devices and human substances from Australia. 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 30, 2023 Other (Non-Commercial) 0 reuses 0 favorites
About the Australian therapeutic goods legislation From Therapeutic Goods Administration (TGA) π¦πΊ Legal requirements for the import, export, manufacture and supply of therapeutic goods in Australia. 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 October 23, 2023 Other (Non-Commercial) 0 reuses 0 favorites
Medical devices: legal requirements for specific medical products From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic 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 July 1, 2023 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Agreement between an organization representing multiple legal manufacturers within a single company and an authorized representative From Saudi Food and Drug Authority (SFDA) πΈπ¦ Agreement between an organization representing multiple legal manufacturers and an authorized representative form. 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 February 16, 2023 Other (Public Domain) 0 reuses 0 favorites
Agreement between a single legal manufacturer and an authorized representative From Saudi Food and Drug Authority (SFDA) πΈπ¦ Agreement between a legal manufacturer and an authorized representative form. 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 February 16, 2023 Other (Public Domain) 0 reuses 0 favorites
Organisation details From Therapeutic Goods Administration (TGA) π¦πΊ This form collects information about the legal entity making applications under the Therapeutic Goods Act 1989. 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 12, 2022 Other (Non-Commercial) 0 reuses 0 favorites
Medical devices: how to comply with the legal requirements in Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ What you need to know before you can place a medical device on the Great Britain market with a UKCA mark. 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 31, 2020 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Medical devices: conformity assessment and the UKCA mark From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ How to conform with the legal requirements for placing medical devices on the market. 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 31, 2020 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Conditions for legal marketing of medical devices From National Institute of Pharmacy and Nutrition (OGYΓI) ππΊ A document outlining the regulations and requirements for the lawful marketing of medical devices. 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 5, 2019 Other (Public Domain) 0 reuses 0 favorites
CPG Sec. 130.200 Inspection of Firms when Legal Action is Pending From Food and Drug Administration (FDA) πΊπΈ CPG Sec. 130.200 provides guidance on inspecting firms when legal action is pending. Metadata quality: Metadata quality: Data description empty 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: 55.55555555555556/100 Updated on December 1, 2018 Other (Public Domain) 0 reuses 0 favorites
Legal Documents for registration in the Electronic Register of Medical Devices From National Organization for Medicines (EOF) π¬π· We would like to inform you that the Table of Legal Entries has been amended ... 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 October 19, 2018 Other (Public Domain) 0 reuses 0 favorites
Human placenta ingestion From Therapeutic Goods Administration (TGA) π¦πΊ Potential health risks and legal implications for placenta consumption 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 January 19, 2018 Other (Non-Commercial) 0 reuses 0 favorites
Clarification of the Term "Legal Entity" for MDSAP Recognition Purposes From International Medical Device Regulators Forum (IMDRF) π Information document IMDRF/MDSAP WG/N29FINAL:2015. 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 October 2, 2015 Other (Public Domain) 0 reuses 0 favorites
Joint European Medicines Agency (EMA), US Food and Drug Administration (FDA), and Japanese Ministry of Health, Labour and Welfare (MHLW) and Pharmaceuticals and Medical Devices Agency (PMDA) orphan medicinal product workshop From European Medicines Agency (EMA) πͺπΊ A workshop on orphan medicinal products organized by EMA, FDA, MHLW, and PMDA. 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 March 28, 2014 Other (Public Domain) 0 reuses 0 favorites