AirTel e-CRFs are planned and realized to fully comply with all GCP, FDA and EMEA requirements for Phase 2-4 Clinical Studies. AirTel e-CRFs can also be used for observational or epidemio- logic studies, where full GCP compliance ...

AirTel e-CRFs grant for total and absolute data traceabi- lity.
No data modification can be performed without multiple and redundant signs of this beeing punctually traced in data records; so precise informations ...

While once we where required to specify the exact number of edit-check implemented in our e-CRF, now it has become clear that every single piece of data that has to be inserted into a Clinical Database, should be carefully cheked ....

Using an e-CRF of Excellence, like an AirTel e-CRF, greatly improves data quality while lowering study monitoring and management costs.
These advantages are similar to those coming, for instance, from modern telecommunication technologies: just think of e-mail, which has dramatically sped up delivery times at costs close to zero