

Operations
Workflows, staffing, and daily site routines.
Regulatory
Processes, documentation, and expectations.
Imaging
Equipment, capture workflows, and data quality.
Sponsors
Expectations before, during, and after startup.
The readiness gap
Becoming a capable research site requires coordinated decisions across staffing, workflows, facilities, equipment, regulatory processes, imaging, data, sponsor expectations, and day-to-day trial operations. The right model depends on the practice—its people, locations, existing capabilities, growth goals, and the types of studies it hopes to support.
Staffing
Workflows
Imaging
Regulatory
Sponsor expectations
What We Do
Focused support for research readiness.
Who We Help
Ophthalmology practices exploring clinical research for the first time.
Practices expanding an existing research program and clarifying what needs to mature next.
Multi-location ophthalmology groups seeking a repeatable research model across sites.
Our Approach
Why Row21
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ABOUT
Row21 helps ophthalmology practices understand what it takes to participate in sponsor-funded clinical trials—and build the people, processes, infrastructure, and operating model required to do it well.
Our approach combines ophthalmic clinical perspective with practical attention to how research must fit within the realities of a working practice.
Next step
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