The Easy CRF technology boosts institutional research:
In the context of intervention research, Easy CRF offers:
CE marking for medical devices : the manufacturer must provide the certification of conformity for the medical device with Directive 93/42 / EEC reinforced by Directive 2007/47/EC.
A device postmarketing surveillance must be in place by the manufacturer. This clinical evaluation will collect clinical data on safety and performance.
Easy-CRF, through specifically created questionnaires, allows you to set up practices, preferences or satisfaction surveys with practitioners, pharmacists and / or patients.
Solicitations for responses to questionnaires can be sent by your teams or by Easy-CRF from your files, your website or your Facebook pages. To ensure optimum compliance, it is possible to answer the questionnaires as well on PC, on tablets or mobile phones.
An evaluation can be composed of several pages whose filling is done according to a schedule set in advance.
With a recovery system in the event of no response, Easy-CRF offers the ability to simply conduct longitudinal and prospective evaluations.
Easy-CRF can provide a study report and proposals for abstracts, if maximum visibility for your results is desired.