Compliance Policy Guide Sec. 390.200 Determination by Secretary that Product Fails to Comply or has Defect - 21 CFR 1003.11 From Food and Drug Administration (FDA) ๐บ๐ธ A document outlining the process for the Secretary to determine non-compliance or defects in products, referencing 21 CFR 1003.11. Part of Compliance Policy Guide (CPG). 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 2 weeks ago Other (Public Domain) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H โ Medical Devices โ Part 800 General From Food and Drug Administration (FDA) ๐บ๐ธ 21 CFR Chapter I Subchapter H - Medical Devices - Part 800 General: A regulation governing medical devices. Metadata quality: Metadata quality: Data description filled Files documented 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: 77.77777777777779/100 Updated on June 4, 2024 Other (Public Domain) 0 reuses 0 favorites
Reporting of serious adverse events and device defects in performance studies with IVDs From Ministry of Health (Italy) (MDS) ๐ฎ๐น 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 May 28, 2024 Creative Commons Attribution 3.0 0 reuses 0 favorites
Reporting of serious adverse events and device defects in performance studies initiated before May 26, 2022 with non-CE marked IVDs From Ministry of Health (Italy) (MDS) ๐ฎ๐น 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 November 28, 2023 Creative Commons Attribution 3.0 0 reuses 0 favorites
CPG Sec. 390.225 Early Defects or Noncompliance - 21 CFR 1004.6 From Food and Drug Administration (FDA) ๐บ๐ธ This document is titled "CPG Sec. 390.225 Early Defects or Noncompliance - 21 CFR 1004.6" and it is a Compliance Policy Guide (CPG). 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 May 6, 2021 Other (Public Domain) 0 reuses 0 favorites
CPG Sec. 345.100 Condoms; Defects - Criteria for Direct Reference Seizure From Food and Drug Administration (FDA) ๐บ๐ธ This document is a Compliance Policy Guide (CPG) titled "CPG Sec. 345.100 Condoms; Defects - Criteria for Direct Reference Seizure". It falls under the topic of "Administrative / Procedural". 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 May 3, 2021 Other (Public Domain) 0 reuses 0 favorites
CPG Sec. 335.800 Clinical Thermometer - Adulteration; Misbranding Defects From Food and Drug Administration (FDA) ๐บ๐ธ This document is a Compliance Policy Guide (CPG) titled "CPG Sec. 335.800 Clinical Thermometer - Adulteration; Misbranding Defects" and falls under the topic of "Administrative / Procedural". 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 May 3, 2021 Other (Public Domain) 0 reuses 0 favorites
The Human Medicines (Amendment etc.) (EU Exit) (No. 2) and the Medical Devices (Amendment etc.) (EU Exit) (No. 2) Regulations 2019 From Medicines and Healthcare products Regulatory Agency (MHRA) ๐ฌ๐ง These Regulations (which come into force immediately before exit day) are made to correct drafting defects and omissions in the Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775) and the Medical Devices (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/791). This isโฆ 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 12, 2019 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites