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The characteristics, diagnosis, management, surveillance and epidemiology of pneumococcal disease.
Information to assist with differentiating Lyme disease from other causes of rash, neurological or non-specific symptoms.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for health protection specialists on the investigation of disease clusters suspected of being caused by exposure to environmental hazards.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on listed diseases of fish and shellfish and their status in England and Wales, including what happens if a disease is suspected or confirmed.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Non-nuclear radioactive substances regulation (RSR), when you need a permit, types of permits, how to apply, change (vary), transfer or surrender your permit.
A guide to non-standard files outside the standard Foreign, Commonwealth & Development Office corporate file plans.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Volume 43 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 10 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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