ZL000_00_036e_WL Guidance document GMP compliance by foreign manufacturers From Swiss Agency for Therapeutic Products (Swissmedic) π¨π Guidance document on GMP compliance by foreign manufacturers. 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 April 15, 2024 Other (Non-Commercial) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H β Medical Devices β Part 803 Medical Device Reporting From Food and Drug Administration (FDA) πΊπΈ This document is a regulation titled "21 CFR Chapter I Subchapter H β Medical Devices β Part 803 Medical Device Reporting". 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 March 31, 2023 Other (Public Domain) 0 reuses 0 favorites
Regulatory Information From Pharmaceuticals and Medical Devices Agency (PMDA) π―π΅ A document discussing regulatory information related to reviews and related 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 April 13, 2024 Other (Public Domain) 0 reuses 0 favorites
Registration Application for Foreign Manufacturers of Medical Devices and In Vitro Diagnostic Products From Pharmaceuticals and Medical Devices Agency (PMDA) π―π΅ A document outlining the registration process for foreign manufacturers of medical devices and in vitro diagnostic products, focusing on assessment-related operations. 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 days ago Other (Public Domain) 0 reuses 0 favorites
Consultations From Pharmaceuticals and Medical Devices Agency (PMDA) π―π΅ PMDA consultations. 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 30, 2024 Other (Public Domain) 0 reuses 0 favorites
Accreditation of Foreign Manufacturers From Pharmaceuticals and Medical Devices Agency (PMDA) π―π΅ This document discusses the accreditation process for foreign manufacturers. 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 10, 2024 Other (Public Domain) 0 reuses 0 favorites