Chapter 4 - nicotine dose guidance Northern Ireland 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. 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 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 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 1.1 - submission type guidance Northern Ireland 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 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 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
Medical devices From European Medicines Agency (EMA) πͺπΊ Medical devices are regulated at EU Member State level, but the European Medicines Agency (EMA) is involved in the regulatory process. 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 May 21, 2024 Other (Public Domain) 0 reuses 0 favorites
Implementation of medical devices future regime From Medicines and Healthcare products Regulatory Agency (MHRA) π¬π§ A roadmap outlining the intended timelines for delivering a future regulatory framework for medical devices and an intended policy on international recognition. 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 3, 2024 Open Government Licence 2.0 (United Kingdom) 0 reuses 0 favorites
Intent to Exempt Certain Unclassified Medical Devices from Premarket Notification Requirements: Guidance for Industry and Food and Drug Administration Staff From Food and Drug Administration (FDA) πΊπΈ This document is a guidance for the industry and FDA staff regarding the exemption of certain unclassified medical devices from premarket notification requirements. 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 June 14, 2019 Other (Public Domain) 0 reuses 0 favorites
Medical Devices; Ophthalmic Devices; Classification of the Eyelid Weight From Food and Drug Administration (FDA) πΊπΈ Document number 2013-02862. The Food and Drug Administration (FDA) is proposing to classify the eyelid weight into class II (special controls). The eyelid weight may be adhered to the outer skin of the upper eyelid (external eyelid weight) or implanted into the upper eyelid (implantable eyelidβ¦ 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, 2013 Other (Public Domain) 0 reuses 0 favorites