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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How a marketing authorisation holder should report a defect with a veterinary medicine.
You can raise an issue about the service you get from a Disability Confident employer.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How we assess issues of potential regulatory concern
The Planning Inspectorate appeals casework portal - Troubleshooting
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Current issues relating to imports and exports of animals and animal products.
Advice on writing clear notices and maximising replies to your FSNs.
Details of appeals which have been chosen by the tax tribunal as lead cases, where there are a number of similar appeals.
Find out more about HMRC's work with these briefings.
How to apply for marketing authorisation via this new procedure.
Use these examples to help you complete declarations on the Customs Declarations Service for exports.
Anyone can report an illegal medicine or prescription misuse and a company can use these forms to report a supply problem or product defect.
Check the availability and any issues affecting the Customs Declaration Services.
This guidance identifies common issues with validation and assessment of clinical trial applications and how to avoid them.
Don’t include personal or financial information like your National Insurance number or credit card details.
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