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Employment Appeal Tribunal Judgment on Recusal Application of Judge Tayler on 30 April 2024.
Decision for applicant Sodexo against registration number 14990935, applicant successful.
Find out about applications to protect traditional terms related to wine products in Great Britain.
How to use a quasi-experimental study to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use a before-and-after study to evaluate your digital health product.
Use these general provisions to help you determine the origin of your products.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How to use a case-control study to evaluate your digital health product.
Read the Council Directive 2003/48/EC of 3 June 2003 on taxation of savings income in the form of interest payments.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
How to use a randomised controlled trial to evaluate your digital health product.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Actions that trial sponsors should consider to build resilience into clinical trial design
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Apply for a higher education course, track your application and accept or reject your offers.
Choose how you’ll make supplementary declarations for goods that you entered into your own records without authorisation.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
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