EUCROF Survey for CRAs training specific for paediatric trials
EUCROF Paediatric Working Group aims to contribute to the improvement of paediatric research by collaborating with the different stakeholders, from the regulatory authorities, to pharmaceutical industry and patient advocacy groups. The working group also aims to increase knowledge related to paediatric clinical research. For this reason, the following survey has been set up with the scope to investigate which topics can be of interest for CRAs in the framework of future training activities.
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PERSONAL DATA
Name and Surname *
Country *
E-mail address *
QUESTIONS
1) Would you be interested in CRA training specific to paediatric trials ?
Clear selection
2) Regarding the training methods, would you be interested in Face to Face training ?
Clear selection
3) Would you be interested in Training as Webinar ?
Clear selection
4) Please, express your interest in the following topics, by indicating a score from 1 to 5 (where 1 means "not all interested" and 5 "extremely interested") *
1
2
3
4
5
Regulatory framework and requirements
Informed Consent and Assent process
Safety
Endpoints
Dosing
Formulation
Samples
Laboratory specificities
Assays
Follow-up of children after end of trial
Parents’ perspective during enrollment and during the study
Differences between age-groups in the management of regulatory aspects, safety, endpoints, dosing, etc
Please, indicate any further topics of interest for you
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