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Pharmacovigilance system requirements
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.
Design, build and operate APIs in a consistent way
The requirements for packaging DNLEU
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 flavour pods.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Check the tariff classification for peptide nisin standardised with sodium chloride
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.
Form to report patients meeting the case definition.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to register as a spring water producer, and the rules you must follow to produce and market spring water.
The diagnosis, management and epidemiology of Bacillus spp.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Regulations to reduce the risk posed by the production, importation and storage of ammonium nitrate.
Check the tariff classification for antimicrobial bathing systems.
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