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Information to support your recovery after COVID-19.
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).
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Use a separate statement of objection form for each Japanese GI product name you object to.
Use this form for SARS-CoV-2 to request sample referrals from your regional public health unit.
Guidance on fixing ClickShare connectivity issues being experienced by users with a MacBook.
Guidance and support on coronavirus (COVID-19) in Scotland.
Information about how many laptops, and tablets and 4G routers we have delivered or dispatched to local authorities, and academy trusts and FE colleges.
Volume 31 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 36 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
This Directorate Children and Young People (DCYP) COVID-19 page provides important advice and updates for service parents.
Crescent Pharma Limited has informed the MHRA regarding an error with the European Article Number (EAN) barcode on the cartons of the above-mentioned batches of Pantoprazole 40 mg Gastro-Resistant Tablets distributed by Crescent Pharma Limited.
Laboratories can use these templates to notify relevant clinicians of a presumed positive blood spot screening result for cystic fibrosis (CF).
Volume 40 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
The quarterly results of the Defence Infrastructure Organisation service delivery customer satisfaction tracker survey.
Volume 38 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Letters from the regulator to registered providers during the COVID-19 pandemic.
Information on variants of the SARS-CoV-2 virus.
Explains testing from 1 April 2024 onwards and sets out the purpose of ongoing testing, who will be eligible to access testing and when tests should be used.
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