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Register to vote Register by 18 June to vote in the General Election on 4 July.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check if you need to tell DVLA about a health or medical condition, how to report medical conditions to DVLA
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
The signs of foot and mouth disease, what to do if you suspect it in your animals and measures to prevent its spread.
Decide which activities are business or non-business for VAT purposes if you're a local authority or other public body.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
This series brings together all documents relating to BIS performance indicators
You may need to tell DVLA if you have a medical condition affecting one or both eyes - report it online or download a form to let them know
Information for clinicians and patients.
Information for patients, healthcare professionals and developers of new medicines
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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