21 CFR Chapter I Subchapter H β Medical Devices β Part 866 Immunology and Microbiology Devices From Food and Drug Administration (FDA) πΊπΈ Regulation on Immunology and Microbiology Devices under 21 CFR Chapter I Subchapter H - Medical Devices, Part 866. Metadata quality: Metadata quality: Data description filled Files documented License filled Update frequency followed File formats are open Temporal coverage not set Spatial coverage filled All files are available Learn more about this indicator Metadata quality: 88.88888888888889/100 Updated 1 day ago Other (Public Domain) 0 reuses 0 favorites
Vapes: information for pharmacists From Therapeutic Goods Administration (TGA) π¦πΊ Learn about changes to the regulation of vapes, what the changes mean for sourcing these products and the requirements for dispensing. 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 19, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Provision No. 2303/2014 From National Administration of Drugs, Food and Medical Devices (ANMAT) π¦π· The Medical Product Traceability System to be implemented by individuals or legal entities involved in the distribution, dispensing and application chain of medical products registered before this National Administration, under the terms set forth in Article 1 and following of the Resolution ofβ¦ 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, 2014 Creative Commons Attribution 4.0 0 reuses 0 favorites
Provision No. 2175/14 From National Administration of Drugs, Food and Medical Devices (ANMAT) π¦π· It is hereby established that individuals or legal entities involved in the chain of marketing, distribution and dispensing or professional application of medical products registered before the ANMAT, shall implement a traceability system to ensure the control and monitoring thereof, from theβ¦ 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, 2014 Creative Commons Attribution 4.0 0 reuses 0 favorites
Ordinance regulating the dispensing of medical devices (Medical Devices Dispensing Ordinance - MPAV) From Federal Ministry of Justice (Germany) (BMJ) π©πͺ MPAV introduces regulations for dispensing medical devices, ensuring safe and controlled distribution. 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 12, 2024 Other (Public Domain) 0 reuses 0 favorites