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Information to support your recovery after COVID-19.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Volume 10 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Volume 13 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 23 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 19 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Healthcare professionals should complete this form for children who are carriers of the cystic fibrosis (CF) gene within 24 hours of giving results.
Volume 4 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Guidance on the national tuberculosis (TB) strain typing service, including its work, achievements, objectives, and future direction.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
Information for clinicians on diagnosis and notification of Shiga toxin-producing Escherichia coli (STEC) and haemolytic uraemic syndrome (HUS).
This series brings together all documents providing updates on standards and technical documents issued by CEN.
You can report serious concerns about your employer to us, if you suspect wrongdoing in an area we regulate.
This guidance provides information on COVID-19 in homelessness, domestic abuse refuge, respite room and asylum seeker accommodation settings.
Laboratories can use this form when requesting a repeat immunoreactive trypsinogen (IRT) test if a first blood spot test is inconclusive for cystic fibrosis (CF).
This webinar looks at the information an organisation makes available to clients, or potential clients, and how the consumer's expectations can be met.
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