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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
UKHSA are providing an update to previous advice regarding contaminated non-sterile alcohol-free wipes in response to continuing detection of cases and a recent death attributable to Burkholderia stabilis infection.
You must not supply certain single-use plastic items in England, except for some exemptions.
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.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Check the tariff classification for Superabsorbent Polymer (SAP) relating to Disposable absorbent training pads for dogs and Bed liners for incontinence patients.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
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