22 September 08:00 - 22 September 17:00
A seminar presenting current thinking on the use of electronic systems in clinical trials, as well as inspection findings that can be attributed to the use of such systems. Speakers are international experts from the British (MHRA), Danish (DHMA), and Swedish (MPA) regulatory agencies as well as from industry, vendors and academia.
For everyone working with or wishing to update their knowledge of regulatory requirements and practical aspects of electronic data handling in clinical trials.
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