International Recognition Procedure From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 How to use the procedure for medicines licensing applications. 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 3 weeks ago Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Presentation: Medical device regulatory lifecycle and clinical evidence requirements From Therapeutic Goods Administration (TGA) 🇦🇺 TGA presentation slides from Queensland Cardiovascular Research Network Webinar (25 June 2021). 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 20, 2022 Other (Non-Commercial) 0 reuses 0 favorites
Converting Centrally Authorised Products (CAPs) to UK Marketing Authorisations (MAs), 'grandfathering' and managing lifecycle changes From Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧 This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products. 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 15, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Multi-stakeholder webinar to support implementation of the Medical Devices Regulation on drug-device combinations From European Medicines Agency (EMA) 🇪🇺 Webinar to aid implementation of Medical Devices Regulation on drug-device combinations for multiple stakeholders. Metadata quality: Metadata quality: Data description filled 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: 66.66666666666666/100 Updated on January 22, 2021 Other (Public Domain) 0 reuses 0 favorites
Useful resources for business and researchers From Therapeutic Goods Administration (TGA) 🇦🇺 This page helps point you in the right direction of where you might go to receive support and information at different stages of the product lifecycle. 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 11, 2020 Other (Non-Commercial) 0 reuses 0 favorites