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Register to vote Register by 18 June to vote in the General Election on 4 July.
Examples of unacceptable trade marks around protected emblems, internet domain names and your company name.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Check what you need to do to sell cosmetic products in Great Britain.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance on how to register, manage and enforce a trade mark. A trade mark protects your brand, for example the name of your product or service.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Use a separate statement of objection form for each Japanese GI product name you object to.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Use a separate statement of objection form for each Georgian GI product name you object to.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for suppliers and dealers.
Use a separate statement of objection form for each Moldovan geographical indication (GI) product name you object to.
Submissions related to human medicines need to be submitted directly to the MHRA.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
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