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Therapeutic Expertise

Ophthalmology

Established Site Network, Rapid
Start-Up, Reliable Outcomes

REV Clinical brings unmatched depth in ophthalmology trials, combining trusted site relationships, strong KOL networks, and seamless execution leveraging our Global Velocity Networkâ„¢. Our team accelerates feasibility, streamlines start-up, and ensures data integrity, delivering reliable outcomes across early- and mid-phase ophthalmology studies.

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Ophthalmology Clinical
Study Capabilities

REV Clinical executes ophthalmology studies end-to-end, from first-in-human to pivotal and post-market, with adaptive design, rigorous oversight, and multi-region operations that accelerate enrollment, uphold quality, and streamline submissions.

  • FIH, Phase I & II studies
  • Dose escalation studies (SAD/MAD)
  • PK/PD interaction studies
  • Biosimilar studies
  • Phase III and Phase IV studies
  • PMS studies
  • Patient registry trials
  • Concept designing, regulatory strategy drafting & FDA communications
  • Confirmatory phase III studies
  • Clinical endpoint studies
  • Pilot studies
  • Pivotal studies
  • Premarket Approval (PMA) trials
  • 510K studies
  • Human factor studies
  • Significant risk (SR) studies
  • Non-significant risk (NSR) studies

Wide Breadth of
Ophthalmology
Indications

REV has experience with both anterior and posterior ophthalmology trials for therapeutics and medical devices. This extensive experience gives our sponsors the flexibility to work with REV across a wide range of ophthalmology trial types.

  • Blepharitis
  • Keratitis
  • Pterygium
  • Pinguecula
  • Chalazion
  • wAMD (Wet AMD)
  • DME (Diabetic Macular Edema)
  • GA (Geographic Atrophy)
  • Diabetic Retinopathy
  • Macular Degeneration
  • Macular Edema
  • Retinal Artery Occlusion
  • Retinal Vein Occlusion
  • Uveitis (Posterior)
  • Mutation-Related Conditions
  • Dry Eye
  • Presbyopia
  • Myopia
  • Astigmatism
  • Conjunctivitis
  • Pterygium
  • Cataracts
  • Glaucoma (Open-Angle)
  • Corneal Ulcer

Established
KOL and Site
Relationships

We have had long-standing relationships with ophthalmology investigators and key opinion leaders across all major subspecialties. This network enables rapid site identification, strong engagement of physician investigators (PIs), and feasibility guided by trusted experts.

Operational Ease

REV’s ophthalmology team has leveraged its leadership team and KOL network to establish a robust approach to ophthalmology clinical trial execution. Sites know REV well, and we know the right investigators, streamlining feasibility, start-up, and execution.

Global Reach

REV fully leverages its U.S., India, and Australia operations for ophthalmology programs, enabling sponsors to conduct credible global or regional trials quickly and cost-effectively.

Ophthalmology Study
Start-Up Services

Perhaps you are waiting for regulatory approvals, additional funding, or the completion of intellectual property filings. REV’s oncology study start-up services can be offered as a standalone service, separate from the operational plan, so that you’ll be positioned to rapidly secure your first patient when you are ready.

01

Finalize your clinical trial design and protocol

02

Create your study’s technology management plan

03

Conduct feasibility outreach and initial site engagement

04

Generate key administrative documentation, like safety management, project management, and medical plans 
Discuss Your Study Start-Up Needs

Regulatory, Quality & Compliance Excellence

REV Clinical’s dedication to excellence is grounded in rigorous process governance, compliance, and an understanding of the regulatory frameworks of the world’s leading regulators.

Let’s Move Your Study Forward

Interested in connecting with REV Clinical’s team of interdisciplinary experts to answer questions, take action on your RFP, and clearly define next steps?

Let's Connect