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Optimize Your Clinical Trials

institutional research

Academic Research

The Easy CRF technology boosts institutional research:

  • Patient reported outcome (PRO) (tablet, smartphone) sent directly by email or given directly to the patient before medical consultation (see below)
  • Investigators may register themselves into your study by utilizing your study URL.
Drug development

Drug development

In the context of intervention research, Easy CRF offers:

  • An online randomization system
  • Flexible management of queries
  • Trace missing data
  • Audit trail of data enteries
  • Record of login/logout
  • Record of page electronic signatures
  • Sending by mail or fax reports of serious adverse events
  • Bilingual English / French
Medical devices

Medical devices

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.


Your surveys

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.