Send and receive information on adverse drug reactions (ADRs)

Name: Send and receive information on adverse drug reactions (ADRs)
Creator: Medicines and Healthcare products Regulatory Agency
License: https://www.nationalarchives.gov.uk/doc/open-government-licence/version/2/
Keywords: authorization,drugs,guidances,marketing,marketing-authorization,medicines,mhra

Information

Original link

Type

Guidance

Regulated products

Medical Devices

Topics

Health And Social Care

Published

December 18, 2014

Last updated

May 9, 2024

Description

How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.

Organization

Medicines and Healthcare products Regulatory Agency (MHRA) 🇬🇧

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

Feedback

Suggest an improvement to this page

1 Main file

Send and receive information on adverse drug reactions (ADRs)

Updated on May 9, 2024

html

URL: https://www.gov.uk/guidance/send-and-receive-information-on-adverse-drug-reactions-adrs
Permalink: https://data.openrid.co/en/datasets/r/f860b192-79f4-41ef-ae6e-a89ed00ce5f2
MIME Type: text/html

Created on: December 18, 2014
Modified on: May 9, 2024

Send and receive information on adverse drug reactions (ADRs)

Information

Type

Regulated products

Topics

Published

Last updated

Description

Tags

Organization

Country / Region

License

Feedback

Actions

Social networks

Embed