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Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
How online marketplaces will deal with VAT for goods from overseas that are sold to customers in the UK.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
Past and current clinical trials into therapeutic and antiviral treatments for COVID-19, how to take part, and which treatments have proven to be effective.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
The prohibitions and restrictions on the import of animal furs and skins into the UK and the export of salmon and trout.
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
Guidance on the many ways for suppliers to work with the Defence Science and Technology Laboratory (Dstl), the science inside UK defence and security.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
Topical steroid products are safe and highly effective treatments for the management of a wide range of inflammatory skin diseases but have important risks, especially with prolonged use at high potency. In the coming months, as a result of regulatory...
How to use a crossover randomised controlled trial to evaluate your digital health product.
Guidance for manufacturers, importers and distributors.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
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