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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
If you’re unsure about an email, letter, call or text you receive from the Insolvency Service, get in touch with us.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Rules employers must follow when making staff redundant - consultations, notice periods, compulsory and non-compulsory redundancy and redundancy pay
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guide includes a selection of environmental and climate considerations to support the rollout of digital infrastructure. It is based on England jurisdiction, but has direct relevance across devolved administrations too.
These include lesson plans for teachers, other resources for the classroom as well as exercises and activities for home learning for both children and adults.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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