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Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Acceptable use policy for the Defence and Security Accelerator online submission service.
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Use this form to submit an article to feature in a future edition of the serious and organised crime (SOC) local partnerships bulletin.
Applicants must obtain a submission slot in advance of submitting selected National Pharmaceutical MA applications.
If you're moving goods outside the UK, you'll need to make an exit summary declaration if you've not fulfilled safety and security requirements with a full customs export declaration.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Annual return form AR27, with guidance for completion.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Tell Companies House about the removal of restriction to amend the company's articles of association.
Instructions on how members of the public can submit their submissions to support the work of the team of experts leading the review.
The Subsidy Advice Unit (SAU) has accepted a request for a report providing advice to DESNZ and DBT concerning the proposed EII Exemption from Nuclear RAB Policy Costs subsidy scheme.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
Pharmacovigilance system requirements
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Get your goods cleared by the National Clearance Hub when moving goods into, out of, or through the UK.
Don’t include personal or financial information like your National Insurance number or credit card details.
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