We will work primarily from a protocol (be it one that we have designed ourselves or a pre-existing document) to produce robust CRF content and collect the essential trial data. This can be done for paper CRFs, or we can deliver complete eCRF solutions through one of our trusted partners.

Too often, clinical teams are presented with messily designed CRFs that do not get to the heart of the primary and secondary endpoints of the study at hand. Ixia’s development and design team prioritise streamlined and neat forms, forgoing extraneous information and ensuring clinical staff at both site and CRO the easiest and most convenient means of data collection, query raising and resolution, discrepancy management, database locking and monitoring possible.