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How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
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.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
Use supplementary pages SA109 to record your residence and domicile status on your SA100 Tax Return.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
Check the patents journal to find UK-registered patents granted, published and filed
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Get help to classify drones and aircraft parts for import and export.
Find out about tax charges on scholarships.
Find out about the additional expenses rules for employees engaged on international work.
Background information and advice on coronavirus (COVID-19) for health and care professionals.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
How to check that a laboratory is allowed to buy ozone-depleting substances (ODS).
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
The New Active Substance Work Sharing Initiative (NASWSI) has successfully approved several medicines through this international collaboration and continues to foster cooperation and strong relationships between its Access partners. The Biosimilar Work Sharing Initiative (BSWSI) builds on this success.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
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