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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Employment Appeal Tribunal Judgment of Lord Fairley on 18 April 2024.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
You must have a legacy-proofing plan for all digital services to prevent the build up of technical debt and future legacy
Bristol-Myers Squibb Pharmaceuticals Limited has informed the MHRA that a potential product quality issue has been detected, relating to incomplete crimping of the metal crimp cap of OPDIVO 10mg/mL concentrate for solution for infusion (nivolumab) (1VLX10ML).
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
medac GmbH (t/a medac Pharma LLP) is recalling the product for the batch specified in this notification due to particles detected during long-term stability tests.
Check the tariff classification for peptide nisin standardised with sodium chloride
Fresenius Kabi Limited has informed the MHRA of an error on the infusion bag packaged into the specific batches of Sodium Chloride Intravenous Infusion 0.9% Freeflex.
Information for HM Passport Office staff about countries and territories beginning with the letters T to Z.
Keep up to date with the UK policy development in respect of Standard Essential Patents.
Product Safety Report for High voltage string lights, HM-E12-1(25) sold via Amazon presenting a high risk of fire.
Volume 40 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Information and guidance for verifying your identity.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Volume 10 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Product Recall for Full Body Detachable Harness sold via eBay presenting a serious risk of injuries.
Volume 33 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
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