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Register to vote Register by 18 June to vote in the General Election on 4 July.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
The seeds which must be certified before you can market them, how to get them certified and how to get a licence for your seed business.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
How to renew marketing authorisations for products granted through different routes and at different times.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to find export opportunities and overseas customers for your business on great.gov.uk: get help selling online overseas, get help from a trade specialist.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
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