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Register to vote Register by 18 June to vote in the General Election on 4 July.
You can send elections, notifications and returns to HM Revenue and Customs by email or electronically to the company’s Shared Workspace.
How to change the ownership from one marketing authorisation (MA) holder to another.
The way you apply to licence biological products has changed
Find out when you can zero rate books and other forms of printed matter.
Cancel a marketing authorisation, traditional herbal registration or parallel import product licence or withdraw a pending submission.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information for people who wish to apply to release a vaccine or a blood product to market in the UK.
This Privacy Notice explains who is processing your data, the personal data we collect, how we use it, who we share it with, and what your legal rights are.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Marking, labelling and marketing standards you must follow to import and export plant seeds, food and manufactured goods.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Pharmacovigilance system requirements
Learn more about off-payroll working rules (IR35) with email updates and recorded webinars.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Our newsletters highlight news and information for all Forestry Commission customers, they are issued via email. National grants and regulations eAlerts are stored on this page.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Over the coming weeks and months, the 'gsi' in email addresses for the Animal and Plant Health Agency will be dropped.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
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