Increase transparency, improve communications and reduce administrative burden for all clinical trial stakeholders.
Even for the most experienced sites, starting up a new study is notoriously inefficient and inordinately burdensome. With protocols and regulations growing in complexity, it’s harder to recruit and retain patients and getting paid takes a valiant effort. Many sites become so overwhelmed by the administrative burden that they withdraw after a single trial, further reducing the pool of investigators available for study opportunities from sponsors.
The Digital Site Suite puts the clinical research site experience at the center of your studies, where it belongs. These industry-leading and award-winning clinical applications give investigators, study coordinators, and site staff the self-serve access to information and documentation they need to run trials with the highest levels of patient focus, compliance and efficiency possible.
减少周期时间,加速站点激活,并保持站点与稳健的工作流程和符合符合性ETMF归档
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