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Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Pharmacovigilance system requirements
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Use this form to file a translation in connection with a European patent or a European patent application
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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
Check the tariff classification for peptide nisin standardised with sodium chloride
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Form to report patients meeting the case definition.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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