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Register to vote Register by 18 June to vote in the General Election on 4 July.
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.
Guidance to aid producers of e-cigarettes and refill containers to prepare notifications for their products.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How to submit a proposal to the Defence and Security Accelerator
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Instructions on how members of the public can submit their submissions to support the work of the team of experts leading the review.
Login or register to the DASA online submission service
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.
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
Submit new evidence if your asylum application has been refused and you have no more right to appeal - called ‘further submission’
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
A party seeking an opinion or determination from the SSRO may find it helpful to complete this submission template and return it to referrals@ssro.gov.uk.
You should follow the standard file process outlined below when submitting work for online and paper billing.
The process to raise matters in relation to the implementation of environment and labour chapters of a Free Trade Agreement.
Guide to the submission process.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The process for applicants applying for a Paediatric Investigation Plan (PIP) modification or waiver.
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