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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Application form ADV1: registration of a person in adverse possession.
Form ST1: Statement of truth in support of an application for registration based upon adverse possession.
Form NAP: notice to the registrar in respect of an adverse possession application.
Application form ADV2: register as a person to be notified of an application for adverse possession.
How marketing authorisation holders should inform the MHRA of a signal or an ADR to a medicine.
The Adverse Weather and Health Plan aims to protect individuals and communities from the health effects of adverse weather and to build community resilience.
Information for manufacturers of Software as a Medical Device, detailing events that may cause indirect harm and are therefore reportable.
Information for public health professionals on immunisation.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Who you should contact if a pet or other animal or human has an unexpected reaction to a veterinary medicine or a problem with a microchip
Advises on how planning can manage potential noise impacts in new development.
Guidance about adverse possession of registered land. Aimed at conveyancers (practice guide 4).
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Guidance on adverse possession where a right to be registered was acquired before 13 October 2003 (practice guide 5).
A report covering adverse reactions to approved COVID-19 vaccines
Form ST2: Statement of truth in support of an application based upon adverse possession of a rentcharge.
For manufacturers reporting adverse incidents with joint replacement implants under the vigilance system.
Don’t include personal or financial information like your National Insurance number or credit card details.
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