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Did you mean Auschwitz prior
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.
Prior Obligations General Licence INT/2023/3024200 and Prior Obligation General Licence Reporting forms
Sections (2.01 - 2.41) last updated January 2024.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Apply to become an approved authorised treatment facility (AATF) and how to operate legally under the approval.
Find out the UK's requirements for the holding and movement of excise goods in duty suspension within the UK and the EU.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Use form C1403 (F) to record changes or clearances of entries input into the Customs Handling of Import and Export Freight (CHIEF) system prior to failure.
You can make observations on the patentability of a published patent application.
Getting a work reference from an employer either while in work or when applying for a new job – and what you can do if you think it's unfair.
What training providers need to do to assess apprentices' prior learning and experience. Including how to record prior learning and calculate price reductions.
The UKHMF Academic Advisory Board provides peer-review and a discussion forum for the Co-Chairs and professional team regarding the envisioned content of the UK Holocaust Memorial and Learning Centre.
Use this form to give notice of final account prior to dissolution in creditors' voluntary liquidation.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
How to find digital outcome, specialist and user research services on the Digital Outcomes and Specialists framework.
Schedule 14 to the Wildlife and Countryside Act 1981 decisions issued by the Planning Inspectorate and published after 1 January 2019
Sections (18.01 - 18.99) last updated: April 2024.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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