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EM Scenarios

This section uses examples of experimental medicine studies to demonstrate how legislative and good practice requirements can be implemented.  Click on a scenario summary below to explore each in full.

Scenarios illustrating the application of the Medicines for Human Use (Clinical Trial) Regulations are not provided on this site.  However the application of best practice to the ‘unregulated’ aspects of an early drug trial (i.e. the use of microbial challenge agents in an early vaccine trial) is given as an example.

This section of the site is a work in progress, as topics are identified, new scenarios will be developed and shared here.

EM Scenarios