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Initiating a clinical trial is a lengthy process, complicated by multiple stakeholders, inaccurate data and complex protocols. The budget creation and negotiation lifecycle today relies on manual, time-consuming workflows which leads to delays. Transforming these processes for clinical trial sponsors and CROs is critical; enabling efficiency and data accuracy can support a streamlined and optimized study start-up, resulting in speed to market, and the delivery of potentially life-saving products to patients that need them.

Today, increased focus has been placed on optimizing elements of study initiation using effective technology - driving process improvement, enhanced collaboration and leveraging reliable sources of data.

You'll discover:

  • How to transform your study start up processes, from site selection, contracting to budget negotiation.
  • How to provide complete confidence in your clinical trial initiation, providing for transparency and management of rates and approvals, ultimately ensuring that your clinical trial is ready for the first patient in.



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