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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A suite of management standards and associated documentation to guide people working in and with the UK government.
How and why you should conduct a right to work check.
Guidance about working in collaboration with other charities.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guide provides advice on using functional standards to support continuous improvement within and across organisations.
Guidance for local authorities in England who are considering adopting a 4-day working week.
What you need to check inside and outside of the vehicle when you do a bus, coach or other public service vehicle (PSV) walkaround check.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
Check if you’re the deemed employer and what your responsibilities are if the off-payroll working rules (IR35) apply.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a quasi-experimental study to evaluate your digital health product.
This guidance is designed to help IT support staff who manage the school's ICT network prepare for check administration.
How to work out the customs value for Customs Duty, import VAT and trade statistics if you’re an importer or clearing agent.
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