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Sun Pharma UK Limited is conducting a precautionary recall of a single batch of Fingolimod SUN 0.5 mg hard capsules due to reports of capsule breakage on removing from the blister. No other batches of Fingolimod SUN 0.5mg hard capsules...
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Zambon SpA is recalling an affected batch as a precautionary measure due to out of specification results for unknown impurities during ongoing stability testing.
Patients implanted with affected devices should expect to be contacted directly for a follow-up assessment, if required.
These documents cover the detail of Public Health England’s (PHE) review of the Nutrient Profiling Model (NPM).
Relonchem Ltd has informed the MHRA that duplicate GTIN numbers have been assigned to certain Losartan potassium/Hydrochlorothiazide coated tablets in error and a duplicate EAN number has been assigned to certain Risperidone tablets in error.
Product Safety Report for Pro Light Skin Lightening Beauty Cream presenting a serious chemical risk.
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