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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.
Remedies form to be completed by merger parties for the offering of undertakings in lieu of reference during phase 1.
How to use an economic evaluation to evaluate your digital health product.
Letters sent by the Competition and Markets Authority (CMA) to companies about their non-compliance with market investigation orders and undertakings.
Exporters must submit a completed end-user and stockist undertaking (EUSU) form when they apply for a standard individual export licence (SIEL) or a standard individual trade control licence (SITCL).
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
This section of the SEPs Resource Hub provides an explanation of SEP specific words and terms used throughout the guidance.
The Company Names Tribunal practice direction provides the framework for the management of proceedings brought before the Tribunal.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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