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List of Field Safety Notices from 22 to 26 April 2024.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Information about the EU Regulations and their implementation in Northern Ireland
Use these forms if you import, export, or move goods through the UK.
Pharmacovigilance system requirements
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use this form to file a translation in connection with a European patent or a European patent application
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to change the ownership from one marketing authorisation (MA) holder to another.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
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