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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance on fixing ClickShare connectivity issues being experienced by users with a MacBook.
Information to support commercial fishers on under 12 metre English vessels.
I-VMS - Frequently asked questions
Guidance and resources to resolve common fingermark visualisation queries and help forensic laboratories achieve and maintain ISO 17025.
This series brings together all documents providing updates on standards and technical documents issued by CEN.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This series brings together all documents relating to September 2012 DFID progress updates on implementing ICAI recommendations
Inspection plans for the Independent Chief Inspector of Borders and Immigration (ICIBI).
Accord-UK Ltd is recalling a specific batch of Co-Codamol 8/500mg Effervescent Tablets (Key Pharmaceuticals Livery) as a precautionary measure due to the internal tablet blister strips being printed with an incorrect expiry date.
Check the tariff classification for articles made of cermet.
Use form FB20 to manually record a schedule of import entries.
How to get fast-track approval of medical devices during COVID-19.
Use this form to record decisions for the recovery of the environment following a radiation incident.
Form for listing all weapons and their serial numbers in the possession of a private maritime security company (PMSC).
Check the tariff classification for empty atomizers.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Explainer for the pharmaceutical industry on Renewal requirements mitigations to bridge the gap between the implementation of the EU Regulation on veterinary medicines and the revised Veterinary Medicines Regulations as they have an effect in Great Britain (GB VMR).
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