The State of Clinical Trial Activation at Sites

Study activation seems like a double-edged sword – before opening a new clinical trial, it is important to craft a detailed and thorough budget, negotiate with the sponsor, receive approvals and sign-offs, and determine protocol feasibility at your site. But all of these important processes take time, resources, and an upfront investment from your sites. So how do sites balance the need to open a study quickly with their regulatory obligations and financial goals?

In order to gain a better understanding of study activation roadblocks, Advarra conducted the Study Activation Report in late 2020. This report reflects survey findings, illustrating key factors affecting study activation, and provides suggestions and solutions to sites wanting to improve their study activation process.

Learn more, download the report today!

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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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