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How investigators and sponsors should manage clinical trials during COVID-19
Make sure that domains that do not send email cannot be used for spoofing.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check how much your visa application costs in the country you’re in
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Use this form to file a translation in connection with a European patent or a European patent application
The family procedure rules are a single set of rules governing the practice and procedure in family proceedings in the high court, county courts and magistrates' courts.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out when and how to take samples for testing, and what happens if one of your flocks tests positive.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Publish your code and use open source to improve transparency, flexibility and accountability.
Use supplementary pages SA109 to record your residence and domicile status on your SA100 Tax Return.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Form to report patients meeting the case definition.
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