- Month 11: strongyloides. we're doing serology for it.
- for the CRF: why are we not using directly tablets for it. We're using paper: it was a matter of cost on one site, the CFR is rather short. Maybe its good a idea to put it on paper and transfer it to the CRF.
- Stella: In terms of regulatory, if Redcap has trazability entonces sí podemos, pero si no no. Is it possible to sign or countersign. That is one of the things you keep hearing.
- EMA has very strict requirements about software for Clinical trials.
- EMA has very strict requirements about software for Clinical trials.
- We can have source documents that are electronic or not, mainly