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Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Pharmacovigilance system requirements
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check the tariff classification for peptide nisin standardised with sodium chloride
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
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.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to get fast-track approval of medical devices during COVID-19.
You must register and declare ozone-depleting substances (ODS) for laboratory or analytical uses.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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