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How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
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.
Information for manufacturers.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
This guide has been produced to assist government and public sector organisations with writing agency briefs when buying communications and marketing services.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
The Writers' Handbook helps writers understand how to use effective writing in their work.
How to use a cost benefit analysis to evaluate your digital health product.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
The team capabilities available on the Digital Outcomes framework.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
How to write requirements for services on the Digital Outcomes and Specialists framework
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
How to use a behaviour change techniques review to evaluate your digital health product.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Don’t include personal or financial information like your National Insurance number or credit card details.
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