Simplifying
Ocular Research
Enhance Your Ophthalmology Research with Expert Clinical Trial Support
From IRB-ready protocols to data analysis and publication-quality manuscripts, Sengi is your partner in clinical research success. Discover tailored solutions that keep your trials on track, compliant, and impactful.
At Sengi, we know that ophthalmology research has unique challenges. Our specialized team supports each step of your study—from protocol drafting to IRB submissions and data analysis—so you can focus on your research’s clinical impact.
Our Expertise in Ophthalmology Clinical Trials
Regulatory Documentation
Streamline the IRB submission process with clear, compliant study protocols, and consent forms.
Data Management & Analysis
Make informed decisions with organized, accurate data that adheres to industry standards.
Medical Writing for Publications
Boost your chances of publication in high-impact journals with expert medical writing that highlights your research’s significance.
Why Sengi?
Our 10 years of experience in ophthalmology clinical trials and close partnership with investigators means you get specialized support, dedicated to ensuring your study’s success and impact.
Delivered On Time
Timing and volume of documentation for clinical trials can be intimidating. We are seasoned professionals who work diligently to meet your deadlines.
Qualified Professionals
The Sengi team is led by medical writer and biostatistician, Dr. Brad Hall. Dr. Hall holds a PhD in Vision Science and Biology.
Confidentiality
We make the security of your research our top priority at every stage of our process.
