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VICH consultation until 15 August 2024 on guidelines relating to the technical requirements for demonstrating pharmaceutical development of veterinary medicinal products.
A. Menarini Farmaceutica Internazionale Srl is recalling a specific batch as a precautionary measure due to the distribution of Invokana 300mg in Northern Ireland in packaging intended for the Greek market.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
The Chief Nursing Officers and Senior Midwives of England, Scotland, Wales and Northern Ireland have spoken out in support of the Tobacco and Vapes Bill.
FCDO travel advice for USA. Includes safety and security, insurance, entry requirements and legal differences.
Principles to support decision making for those involved in safely planning and protecting visiting during outbreaks of infectious illness in adult social care.
This guidance provides information on COVID-19 in homelessness, domestic abuse refuge, respite room and asylum seeker accommodation settings.
Use this form for SARS-CoV-2 to request sample referrals from your regional public health unit.
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 surface-active preparation for washing the skin and the hair (gel 2-in-1).
Information on variants of the SARS-CoV-2 virus.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
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.
This form is for persons affected by a ship's specification or designation to request a review
Information on COVID-19, including guidance on the assessment and management of suspected UK cases.
Information relating to the procurement of the Aerial Dispersant Spray service including background information, upcoming events and links to resources.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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