Streamlined Start-Up Processes

Centralized study initiation activities and digitized source, regulatory, and records management.

Standardized processes to drive streamlined start-up

Velocity goes well beyond the traditional site network or site management organization (SMO) model. By applying a systematic approach to the way sites are built and overseen, Velocity can quickly initiate studies while ensuring operational excellence, even for the most complex trials. For example, with digitized source, regulatory, and records management, Velocity can quickly start, scale, and optimize your study operations as needed.

Beyond accommodating the soft infrastructure required to support your study, Velocity can also integrate new or unique technologies or treatment approaches to run specialized, decentralized, and/or hybrid trials.

• ≤30 days from study award to site initiation visit
• PBMC processing capabilities and on-site labs for some sites
• Integrated tech for payment/stipends, eReg, EMR/HER, same-day collection/shipping
• Study start-up training meetings with site staff
• A clinical data specialist is assigned to every study
• Alignment with your central IRB or central laboratory