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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Learn how to check if your website or mobile app is accessible.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Apply for protection against infringements of intellectual property rights on UK imports and exports.
How legal industrial action is organised, picketing and the law and what your employment rights when you are on strike
What to do if you think someone's used your intellectual property without permission - types of intellectual property abuse, help resolving disputes and further legal action you can take.
The Department for Education's (DfE) sustainability leadership and climate action plans initiative.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This Cold-Health Alert (CHA) action card summarises the suggested actions that voluntary and community sector (VCS) organisations should consider to prepare for and respond to each type of CHA.
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