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How to submit a proposal to the Defence and Security Accelerator
Make building control applications to any local authority in England, Wales or Northern Ireland.
How to submit an application, data package and company responses for proposed or existing authorisations in the UK.
Submissions related to human medicines need to be submitted directly to the MHRA.
Submission dates and how the submissions using the EC decision reliance procedure work.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Webinars for pharmaceutical companies, clinical trial sponsors, e-cigarette producers and brokers of medicinal products
How to use the HM Land Registry Pre-submission Enquiry Service and Application Management Service.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Login or register to the DASA online submission service
Submit new evidence if your asylum application has been refused and you have no more right to appeal - called ‘further submission’
Find out how to submit your research to Athena, Dstl's central repository of MOD-sponsored scientific and technical research reports.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Submit or respond to online applications for certain civil, family and tribunal cases.
Applicants must obtain a submission slot in advance of submitting selected National Pharmaceutical MA applications.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Submission of notifications for northern Ireland under article 20 of directive 2014/40/EU.
5 quick tips on submitiing your paper for review
Guide to the data submission process
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