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Learn more about your responsibilities if you're running a small business including registration, tax returns, record keeping, tax bills and payments.
Webinars for pharmaceutical companies, clinical trial sponsors, e-cigarette producers and brokers of medicinal products
Learn more about the support available to tax agents and advisers which will help you and your clients.
The Office of Financial Sanctions Implementation runs webinars and events to provide guidance on financial sanctions.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Learn more about VAT including accounting schemes, VAT Returns and keeping records.
Find out about exporting products of animal origin (POAO) such as meat, dairy and fish, live animals, plants and plant products.
Learn more about getting started as an employer or running a small business including registration, payroll, tax returns, tax bills and payments.
Learn more about money laundering regulations and your responsibilities including the fit and proper test and approval process and report suspicious activity.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
Join our latest webinar with advice on how to file mortgage charges online, and how to register as a lender to file against any company.
Submissions related to human medicines need to be submitted directly to the MHRA.
Learn more about paying tax and keeping records as a property landlord.
Learn more about getting started with Self Assessment including registration, tax returns, tax bills and payments.
Learn more about Making Income Tax and VAT Digital if you’re an agent or a business.
Learn more about paying tax and record keeping for the Construction Industry Scheme if you’re a contractor or subcontractor.
Register now to find out more about what you need to consider when starting a company.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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