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Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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.
Submissions related to human medicines need to be submitted directly to the MHRA.
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply the government secure email policy.
How to apply for marketing authorisation via this new procedure.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How veterinary medicines can be advertised.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Check a list of recent emails from HMRC to help you decide if the email you've received is a scam.
How to sign up for our email reminders service which tells you when your company’s accounts and confirmation statements are due.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
Find out which postage stamps are free of VAT and when VAT must be applied to stamps, stamped stationery and other philatelic supplies.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Pharmacovigilance system requirements
How to change the ownership from one marketing authorisation (MA) holder to another.
Find out when you can zero rate VAT for advertisements and goods used for the collection of donations.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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