Central Laboratory Solutions

Central Laboratory Solutions

Remember the time when laboratory kits were ordered and reordered by sites faxing pieces of paper, and laboratory reports were faxed and express-mailed to investigative sites around the world? Sadly that time is still here for many central laboratory providers.

However, the time has come to reduce study costs for both you and the study sponsors who ultimately pay the cost of these development programs. Trial Interactive has assisted many central laboratory providers in eliminating the need to express-mail documents. We streamline the order and reorder process with a global interface custom-tailored for global clinical studies. With Trial Interactive's real-time access to user activity, you have full visibility into whether your investigative site staff reviewed the critical laboratory reports—allowing you to rapidly improve regulatory compliance.

Configurable workflows can help your project teams manage your investigative sites more effectively while robust reporting provides your sponsor or CRO with real time status on central laboratory activities, reducing your time spent on project management. We have eliminated costs for other central laboratory providers and study stakeholders.

To find out more about how Trial Interactive can assist you with reducing your clinical development costs, contact us.



21 CFR Part 11

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