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A range of tests are available from the majority of PHE regional clinical microbiology laboratories.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a cost effectiveness analysis to evaluate your digital health product.
This document explains the NHS view on private screening for different conditions and diseases.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidelines on sampling and result interpretation for microbiologists and infection control nurses working in healthcare environments.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
How health app content should be reviewed by subject matter experts.
Information on taking, submitting and processing samples which potentially contain monkeypox virus.
The UK Health Security Agency (UKHSA) provides proficiency testing (PT) schemes, also known as external quality assessment (EQA) schemes.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Information on the programme, including commissioning, quality assurance, education and training.
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