ZL000_00_029e_WL Guidance document Packaging texts for veterinary medicinal products From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭 Guidance document on packaging texts for veterinary medicinal products. 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 3 weeks ago Other (Non-Commercial) 0 reuses 0 favorites
ZL000_00_021e_WL Guidance document Packaging for human medicinal products From Swiss Agency for Therapeutic Products (Swissmedic) 🇨🇭 Guidance document on packaging for human medicinal products. 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 August 1, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Guideline on plastic immediate packaging materials From Therapeutic Goods Administration (TGA) 🇦🇺 We have adopted this International Scientific Guideline - CPMP/QWP/4359/03, EMEA/CVMP/205/04 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 18, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Principle 3: Medical devices to be suitable for intended purpose From Therapeutic Goods Administration (TGA) 🇦🇺 Principle 3 requires manufacturers to ensure their devices perform in the way intended. This includes the design, manufacturing process, and packaging. 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, 2024 Other (Non-Commercial) 0 reuses 0 favorites
21 CFR Chapter I Subchapter H – Medical Devices – Part 820 Quality System Regulation From Food and Drug Administration (FDA) 🇺🇸 This document is a regulation titled "21 CFR Chapter I Subchapter H – Medical Devices – Part 820 Quality System Regulation". 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
21 CFR Chapter I Subchapter H – Medical Devices – Part 800 General From Food and Drug Administration (FDA) 🇺🇸 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
Medical devices Unique Device Identification (UDI) From Therapeutic Goods Administration (TGA) 🇦🇺 Labelling and packaging information about medical devices Unique Device Identification (UDI). 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 2, 2024 Other (Non-Commercial) 0 reuses 0 favorites
UDI labelling for sponsors and manufacturers From Therapeutic Goods Administration (TGA) 🇦🇺 Understand and apply the UDI labelling and packaging requirements to your 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 March 26, 2024 Other (Non-Commercial) 0 reuses 0 favorites
Commission Implementing Decision (EU) 2024/817 of 6 March 2024 amending Implementing Decision (EU) 2021/1195 as regards harmonised standards for sterilisation of health care products and packaging for terminally sterilised medical devices From European Parliament 🇪🇺 The document is an EU Implementing Decision from 2024 amending standards for sterilization of healthcare products and packaging for medical 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 March 6, 2024 Creative Commons Attribution 4.0 0 reuses 0 favorites
Commission Implementing Decision (EU) 2024/815 of 6 March 2024 amending Implementing Decision (EU) 2021/1182 as regards harmonised standards for medical gloves for single use, biological evaluation of medical devices, sterilization of health care products, packaging for terminally sterilized medical devices and processing of health care products From European Parliament 🇪🇺 The document is a Commission Implementing Decision amending standards for medical gloves, biological evaluation of devices, sterilization, packaging, and processing of healthcare products. 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 6, 2024 Creative Commons Attribution 4.0 0 reuses 0 favorites
Unique device identification system From Ministry of Health (Italy) (MDS) 🇮🇹 The unique device identification system ("UDI system") provided for in the Medical Devices Regulation (EU) 2017/745 and the In Vitro Diagnostic Devices (IVD) Regulation (EU) 2017/746 allows for the identification and facilitates the traceability of devices. The system involves: assigning a basic… 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 February 12, 2024 Creative Commons Attribution 3.0 0 reuses 0 favorites
Labelling and packaging From Therapeutic Goods Administration (TGA) 🇦🇺 Regulatory information on the labelling and packaging of medicines and 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 21, 2023 Other (Non-Commercial) 0 reuses 0 favorites
State Drug Administration Comprehensive Department on agreeing to prepare for the establishment of medical device packaging standardization technology focal point of the letter From National Medical Products Administration (NMPA) 🇨🇳 FGWJ-2023-10001 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 24, 2023 Other (Public Domain) 0 reuses 0 favorites
Therapeutic goods orders From Therapeutic Goods Administration (TGA) 🇦🇺 Therapeutic goods must comply with various standards, which determine the consistency of product quality, including label quality. Many of these standards are international standards. However, sometimes it is necessary to specify an Australian standard, either for a particular type of therapeutic… 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 30, 2022 Other (Non-Commercial) 0 reuses 0 favorites
Infrared (IR) thermometers: caution in use From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 The MHRA has become increasingly aware of infrared thermometers being sold in the UK that do not comply with the regulations. 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 27, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Commission Implementing Decision (EU) 2021/611 of 14 April 2021 amending Implementing Decision (EU) 2020/438 as regards harmonised standards on biological evaluation of medical devices, packaging for terminally sterilised medical devices, sterilisation of health care products and clinical investigation of medical devices for human subjects From European Parliament 🇪🇺 Commission Implementing Decision (EU) 2021/611 amends Implementing Decision (EU) 2020/438 on harmonised standards for medical devices and clinical investigations. 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 April 14, 2021 Creative Commons Attribution 4.0 0 reuses 0 favorites
Commission Implementing Decision (EU) 2021/610 of 14 April 2021 amending Implementing Decision (EU) 2020/437 as regards harmonised standards on medical vehicles and their equipment, anaesthetic and respiratory equipment, biological evaluation of medical devices, packaging for terminally sterilised medical devices, sterilisation of health care products, clinical investigation of medical devices for human subjects, non-active surgical implants, medical devices utilising animal tissues and their derivatives, electroacoustics and medical electrical equipment From European Parliament 🇪🇺 Amendment to Implementing Decision (EU) 2020/437 on harmonised standards for medical vehicles, equipment, and 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 April 14, 2021 Creative Commons Attribution 4.0 0 reuses 0 favorites
Commission Implementing Decision (EU) 2021/609 of 14 April 2021 amending Implementing Decision (EU) 2020/439 as regards harmonised standards on packaging for terminally sterilised medical devices and sterilisation of health care products From European Parliament 🇪🇺 Commission Implementing Decision (EU) 2021/609 amends standards on packaging for sterilised medical devices and sterilisation of healthcare products. 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 April 14, 2021 Creative Commons Attribution 4.0 0 reuses 0 favorites
Code of practice for tamper-evident packaging of therapeutic goods From Therapeutic Goods Administration (TGA) 🇦🇺 A new version of the code of practice for tamper-evident packaging of therapeutic goods is now available 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 May 18, 2017 Other (Non-Commercial) 0 reuses 0 favorites
42DK(2) Permitted representation: Hospital grade disinfectant or household grade disinfectant From Therapeutic Goods Administration (TGA) 🇦🇺 Guidance document on labelling and packaging requirements for hospital grade or household grade disinfectants. 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 17, 2014 Other (Non-Commercial) 0 reuses 0 favorites