Clinical Trials

Our service offering has been designed to make trials run smoother and operate at scale.

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E-Nome’s system fundamentally changes the relationship between trial participant and sponsor, by introducing secure and automated processes for collection, supplementation and verification of data.

Stage one

Trial participant onboarding

Prior to undertaking the clinical trial there is a pre-trail research and data requirement that ultimately leads to the recruitment and on-boarding of participants.

E-Nome has designed a remote and face to face onboarding process that significantly increases efficiency for sponsors and investigators.

Stage two

Trial communication and end of trial data sharing

Once a participant is on-boarded, the E-Nome system can facilitate all relevant protocol communication.

At the end of a trial, a trial sponsor can easily share relevant trial data if requested and as required.

Stage three

Pharmacovigilance

A secure link between the trial participant and the trial sponsor can be maintained indefinitely, if agreed. Thus enabling rigorous pharmacovigilance to satisfy regulatory requirements.

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