Study design and start-up

Clinical
study start-up

Clinical study start-up is a complex and highly regulated part of a clinical trial involving several stakeholders (sponsor, site, regulatory authorities, etc.). Study start-up includes many milestones starting with feasibility and ending with the enrollment of the first subject, with several activities in-between such as site selection, pre-study visit, regulatory submissions, site contract and budget negotiation, vendor set-up, and site activation.

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Clinical study start-up
Feasibility and site evaluation
Regulatory submissions
Site management
Clinical monitoring

Clinical study start-up

Set-up for success

A successful clinical study start-up is a crucial first step and an important factor for the overall success of the trial. For this reason, SCRO has experienced study start-up teams, offering customized services depending on your needs, whether it be full-service or single activities.

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