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This is guidance on the safe use of ultrasound gel to reduce risk of transmission of infection during ultrasound and related procedures.
Advice for manufacturers of Class I medical devices for placing products on the UK market
This research is an output from the Drugs for Neglected Diseases (DNDi) initiative
This consultation asks for feedback in relation to the bacteriology SMI ‘B 26: investigation of fluids from normally sterile sites.’
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
This paper analyses implications for inflation, output and the exchange rate in the presence of domestic and external shocks
Guidance on decontamination and infection control, including surgical instruments, dental equipment, endoscopes and benchtop steam sterilizers.
BD have notified the MHRA that the sterility of some of their devices cannot be guaranteed due to quality issues with their third-party sterilisation provider.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Information and guidance on group A streptococcal infections.
Cytoplasmic male sterility (CMS) breeding systems expedite the production of hybrid seed in many crops
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