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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Advice on writing clear notices and maximising replies to your FSNs.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Correct the original registration with the register office or GRO - find out what corrections can be made, who can apply, how long it takes, what they look like
What to expect if you're sent to prison - prison rules and regulations, healthcare and education, prisoner rights
Correct an original registration with the register office or GRO - what corrections can be made, who can apply, how long it takes
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Forms and guidance for professionals working with restricted patients (mentally disordered offenders).
How offender healthcare is managed in prisons and in the community.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Policy and guidance for prison and probation professionals in England and Wales.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Use this form to commission a psychiatric or other kind of medical report to help inform sentencing.
This guide provides information about being arrested in Turkey and what conditions are like in prison there.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
This guide provides information about being arrested in Germany and what conditions are like in prison there.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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