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Look up a trade mark to see if something identical or similar to your brand is already registered.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Information for clinicians and patients.
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.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
How to use A/B testing to evaluate your digital health product.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Data on the real-world efficacy of the COVID-19 vaccines.
How to get fast-track approval of medical devices during COVID-19.
Information on variants of the SARS-CoV-2 virus.
How to spot Aujeszky’s disease, what to do if you suspect it and measures to prevent its spread.
Volume 29 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
If you're an employer based in the UK, find out if an employee is eligible for tax relief through an Appendix 5 arrangement if they've paid tax abroad on their income.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Find out about non-cash benefits in connection with termination of employment or from employer-financed retirement benefits scheme
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
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