OptymEdge, part of the Emmes Group, unveiled the clinical research industry's first technology platform dedicated exclusively to ophthalmology trials during ARVO 2025, held from May 4-8. This launch represents the first phase of a comprehensive rollout designed to enhance trial efficiency, improve data quality, and transform OptymEdge into a full-service ophthalmic research partner.
The initial release focuses on Best Corrected Visual Acuity (BCVA) assessment, with additional visual function assessments planned for future development phases. The platform addresses long-standing challenges in ophthalmology trials by replacing paper-based workflows with digital systems.
Digital Transformation of Ophthalmology Trials
The newly launched eSource platform eliminates manual BCVA data entry methods that have traditionally been prone to inconsistency and human error. The system guides users through step-by-step assessment protocols, significantly reducing examiner variability while enhancing data integrity.
"For over 30 years, we've been at the forefront of BCVA certification in ophthalmic clinical trials," said Saqib Parkar, managing director at OptymEdge. "We saw a need to improve data quality, consistency, and efficiency by developing purpose-built technology platforms from the ground up. Our new eSource platform addresses long-standing challenges in manual BCVA data collection and marks a pivotal step in our transformation into a comprehensive ophthalmic research partner."
A key feature of the platform is its full compatibility with Electronic Data Capture (EDC) systems, enabling secure, automated transfer of patient data without creating additional administrative burden for trial sites. This integration streamlines the research process and helps maintain data integrity throughout the trial lifecycle.
Comprehensive Development Roadmap
The platform demonstration at ARVO 2025 represents just the first phase of OptymEdge's strategic expansion. Future development phases will introduce:
- AI-enhanced image analysis tools for trial image reading
- A comprehensive digital network map of global ophthalmology trial sites
- Reading center services for standardized, high-quality image grading
- A global ophthalmology trial site network
These planned enhancements reflect OptymEdge's evolution from a certification provider to a comprehensive research partner capable of supporting both large and small sponsors with end-to-end ophthalmic research services.
Addressing Industry Challenges
The ophthalmology clinical trial landscape has long faced challenges with data consistency, examiner variability, and manual workflows. OptymEdge's platform directly addresses these issues by standardizing assessment procedures and digitizing data collection.
The company's decades of experience in BCVA certification and visual function endpoint expertise provides a unique perspective on operational challenges in ophthalmology trials. This foundation has informed the development of purpose-built solutions that align with real-world research needs.
"As we expand beyond BCVA into additional ophthalmology endpoints, we're committed to delivering greater standardization, scalability, and value to our partners through integrated digital solutions," added Parkar.
Industry Impact
The introduction of this dedicated platform represents a significant advancement for ophthalmology clinical research. By combining specialized technology with deep domain expertise, OptymEdge aims to deliver a more streamlined, future-ready approach to drug development in the ophthalmology space.
The platform's ability to enhance data quality while reducing site burden addresses two critical challenges in clinical research. For sponsors, this translates to more reliable study outcomes and potentially faster development timelines. For research sites, the platform offers workflow improvements that can enhance efficiency and reduce administrative overhead.
As OptymEdge continues to expand its service offerings in the coming months, the company is positioning itself as a unified, scalable partner for conducting ophthalmology research across the development spectrum.
