Each day a drug with an average sales potential is delayed during the clinical trial process, the sponsor loses an estimated $1.5 million in revenue as the timeframe of market exclusivity shrinks and more importantly, life-saving drugs are kept from patients who could benefit from these new discoveries. We understand how important it is to respect your clinical trial workflow considerations and timelines.

Projects commence with you providing:

• Your trial protocol

• All corresponding paper case report forms

• List of basic edit checks

• Database specifications (for data export)

• Any special reporting requirements

Then, OmniComm's expert Software Development Staff and Clinical Research Associates work closely with you to refine the application/reports and ensure that the TrialMaster application is customized to meet your specific needs.

Once TrialMaster has been configured, OmniComm provides training, either through a "train-the-trainer" program, through broad training sessions for field and home office associates and/or through "trial start-up" meetings. Training generally takes about 1 hour.

Throughout the clinical trial process, OmniComm delivers timely, professional support with the responsiveness you expect from an in-house IT department