CRO Partner for Ophthalmology Clinical Trials

Clinical trials in ophthalmology are unique and differ from other areas of clinical research, with their own challenges in healthcare organization and diseases’ specifics. Recent years have seen a range of exciting new therapies that address the unmet needs of patients, including innovative medications and medical devices to treat age-related conditions, paediatric eye disorders, as well as rare or genetic conditions. Clinical trials remain the only way to bring those innovations to the market. They demand a seasoned team, whether internal or external, to manage the process.

Dokumeds' ophthalmology CRO services can efficiently support all of your development needs for ophthalmic drugs and devices. We have years of continuous experience in ophthalmology clinical trials management and organization, excellent connections with European sites and KOLs, and regulatory specifics knowledge on the regional and local level.

Working continuously with ophthalmology projects since 2000

30 awarded phase II, IV & device projects
Isolated feasibilities performed in an additional 35 projects
Services in ophthalmology provided across 18 countries (EU and non-EU)
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Includes clinical trials in paediatric populations

Main focus areas:

  • Glaucoma
  • Diabetic Retinopathy
  • Cataracts
  • Age-related Macular Degeneration (AMD)
        - Dry AMD
        - Neovascular (wet) AMD
  • Diabetic Macular Edema (DME)
  • Medical devices (lenses, implants, stents)
  • Diabetic Macular Edema (DME)
  • Neovascular Age-related macular Degeneration (wet-AMD)
  • Intra-ocular lens
  • Stent device for glaucoma treatment
  • Diabetic Macular Edema (DME)
  • Neovascular Age-related macular Degeneration (wet-AMD)
  • Intra-ocular lens
  • Stent device for glaucoma treatment

Connected services

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Clinical Operations
Our highly nuanced approach that accounts for the specific needs of each project.
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Supply & Logistics
An established and cost effective logistics supply chain.
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Pharmacovigilance Icon
Pharmacovigilance
We deliver high-quality solutions, with services designed to ensure patient safety at every stage of the drug life cycle.
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Regulatory Affairs
Practice-based regulatory consulting expertise, and support throughout the product life cycle.
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