Selection and cooperation with CRO

Cooperation with a CRO – what agreements are concluded and how are changes managed? RFP in a clinical trial – how to prepare it to choose the right CRO partner? How does communication work in a clinical trial? The roles of the CRA, PM and Sponsor Is every CRO the same? Does experience in a specific trial phase really matter? One CRO or multiple partners? Why the single-CRO model is increasingly winning in clinical trials Quality Under Control: Onsite, Remote Audits, and GDPR Compliance in CRO Operations How to assess whether a CRO has adequate operational resources to run a large-scale or highly complex project? How does a CRO manage relationships with investigative sites and ensure the quality of data collected at sites? What are the typical collaboration models between a CRO and a Sponsor? How to oversee the quality of services provided by a CRO? What aspects of collaboration with a CRO have the greatest impact on the quality of a study? What tools and IT systems are used to manage a study? Who is included in the project team proposed by the CRO? How to choose the right partner and build an effective collaboration? What experience should a CRO have to conduct a clinical trial? What criteria should CROs meet when participating in a tender? Does the CRO have experience with publicly funded clinical studies? Does the CRO have experience in a specific therapeutic area?