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Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How local authorities should report data for the annual special educational needs survey, commonly known as SEN2.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Sets out process and expectations on pre-application discussions.
Information to help you identify if your organisation needs to publish a modern slavery statement.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Our self-service training package will help you with the basics – whether you’re new to conveyancing or just need a refresher. This includes working with HM Land Registry, and preparing and submitting high-quality applications.
Find out what you need to do when making a full declaration to send goods from the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This self-assessment checklist helps academy trusts check they are managing resources effectively and identify any adjustments they need to make.
The MHRA is continuing to accept Active Substance Master Files (ASMFs) and Certificates of Suitability (CEPs)
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.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Submit an ERS return if you’re an employer or an agent.
Supports effective delivery of planning application process.
Certification for Good Quality CHP and CHPQA financial incentives.
Submissions related to human medicines need to be submitted directly to the MHRA.
Get your goods cleared by the National Clearance Hub when moving goods into, out of, or through the UK.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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