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FCDO travel advice for the Dominican Republic. Includes safety and security, insurance, entry requirements and legal differences.
Share your reference data for use in projects and services outside your organisation.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
Information about the workflow in Whitehall publisher, and how to review documents including the '2i' process.
Guidelines for civil panel counsel, revised to include the new government security classifications.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
You're required to keep records for all traded goods you declare to HMRC for four years, for duty and tax purposes and for government statistics.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
This is collated guidance from government websites and independent bodies to help you follow the technology code of practice.
A suite of template legal documents to support the development of mutuals.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Accessible documents at Companies House.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
Find the best guidance and tools to meet the accessibility regulations.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Accessible documents at the Department of Health and Social Care.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Don’t include personal or financial information like your National Insurance number or credit card details.
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