We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How to send your information to Companies House using our online services.
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
Guide to the submission process.
Use this form to submit a second filing to correct a very minor inaccuracy in a previously delivered document.
Tell Companies House about the removal of restriction to amend the company's articles of association.
You should follow the standard file process outlined below when submitting work for online and paper billing.
Tell Companies House about a restriction to amend the company's articles of association.
How to submit an application, data package and company responses for proposed or existing authorisations in the UK.
Making changes to your company - passing resolutions, changing addesses and where your records are kept, your company name and type, directors' and secretaries' details, share structure, constitution
Types of model articles of association a limited company can have, including older versions of Table A from previous company legislation.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to file an update statement for an overseas entity and its beneficial owners or managing officers.
Pharmacovigilance system requirements
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Form and guidelines for authors applying to publish in the 'Chemical hazards and poisons (CHaP) report'.
How to submit a proposal to the Defence and Security Accelerator
Submission dates and how the submissions using the EC decision reliance procedure work.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.