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How to use A/B testing to evaluate your digital health product.
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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to use a cost benefit analysis to evaluate your digital health product.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Information about next steps when you have sponsored a guest for 6 months.
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Your chances of obtaining a useful patent are significantly greater if you use an attorney. A patent specification is a legal document and requires specialist skills to draft properly.
The Ministry of Defence (MOD) is committed to making it easier for new, innovative, and smaller businesses to enter the defence supply chain.
How to use a behaviour change techniques review to evaluate your digital health product.
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.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
Learn about about importing and exporting goods.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
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Learn more about Making Income Tax and VAT Digital if you’re an agent or a business.
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