Chapter 4 - nicotine dose guidance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ How to test and report levels of nicotine uptake when submitting a notification of intent to market e-cigarette and vape products in Great Britain. 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 August 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Chapter 3 - emissions guidance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ The types of emissions a manufacturer or importer of e-cigarettes should notify us about. 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 August 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Chapter 2 - product type guidance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Which product type to select when submitting a notification of intent to market e-cigarette and vape products in Great Britain. 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 August 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Chapter 10 - general advice on vigilance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Collecting and acting on information on any adverse effects of electronic cigarette devices and refill containers on human health. 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 August 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Chapter 1 - submission type guidance - Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Which submission type to select when submitting a notification of intent to market e-cigarette and vape products in Great Britain. 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 August 16, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Register medical devices to place on the market From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland 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 August 2, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Borderlines with medical devices and other products in Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Guidance on whether or not your product is a medical device. 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 8, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Regulating medical devices in the UK From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. 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 8, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
The Medical Devices (Amendment) (Great Britain) Regulations 2023 From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ These Regulations amend the Medical Devices Regulations 2002 (S.I. 2002/618) (βthe 2002 Regulationsβ) to extend the periods for which certain medical devices that comply with EU legislation can be placed on the market in Great Britain. The 2002 Regulations were made under section 2(2) of theβ¦ 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 June 9, 2023 Open Government Licence 3.0 (United Kingdom) 0 reuses 0 favorites
Guidance on the licensing of biosimilar products From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ This guideline is to provide developers of biosimilar products with a clear outline of the requirements in Great Britain. 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 November 7, 2022 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Guidance for retailers: supplying medical devices to Northern Ireland From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ How the supply of medical devices from Great Britain into Northern Ireland works. 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 5, 2021 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Medical devices: how to comply with the legal requirements in Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ What you need to know before you can place a medical device on the Great Britain market with a UKCA mark. 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 31, 2020 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
In-house manufacture of medical devices in Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ Guidance for healthcare establishments that manufacture medical devices in-house. 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 31, 2020 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Custom-made medical devices in Great Britain From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ How to comply with the regulatory requirements for manufacturing custom-made 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 31, 2020 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites