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7 months ago · c05965cec4
parent 64112999cc
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 - EMA has very strict requirements about software for Clinical trials.
 - We can have source documents that are electronic or not, mainly a matter for the teams at GHS and KEMRI.
 - The priority is to get the work done and then. We might not do it daily and then the forms will be entered later.
+- Detection of rare adverese events with a frequency with 1/3000.
+- 75 participants from each school para hacer la parte dle estuio relacionada con eficacia.
+-