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How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
This advice gives examples of what the Planning Inspectorate considers to be helpful examples of documentation produced in the Planning Act 2008 process.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Spreadsheets are a common way to share data. Use this information to help you avoid common errors, improve interoperability and create more accessible spreadsheets.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The information clients, principal designers, principal contractors and accountable persons need to keep.
Submit your research to Athena; Dstl's central repository of MOD-sponsored scientific and technical research reports.
Apply for a High Potential Individual (HPI) visa if you've been awarded a qualification by an eligible university in the last 5 years - eligibility, fees, documents, switch, bring your partner and children
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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