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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
All private sector businesses that want to do building control work in England and Wales under the Building Act 1984 (as amended) must apply to register with the Building Safety Regulator (BSR).
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Submit your research to Athena; Dstl's central repository of MOD-sponsored scientific and technical research reports.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
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