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List of currently authorised veterinary medicines containing controlled drugs (CDs) and their requirements for special storage and witnessed destruction.
As with any medicine, the MHRA will keep the safety and effectiveness of sevabertinib under close review.
How manufacturers in Northern Ireland should undertake a clinical investigation for medical devices to ensure they comply with EU medical device regulations.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A change to UK VAT law to permit the zero-rating of the dispensing of drugs prescribed by physiotherapists and podiatrists.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Advice and guidance on the health needs of migrant patients from Paraguay for healthcare practitioners.
Guiding principles for the use of predetermined change control plans (PCCPs) for managing rapid product changes in medical devices.
Guidance on transitional arrangements for the Clinical Trials Regulations.
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