Ophthalmic Clinical Trial Investigator Network

For over 30 years, Ora has been accelerating the pace and improving the quality of allergy research worldwide, earning our clients 19 FDA product approvals along the way. At Ora, your ophthalmic clinical research programs are backed by the experience and expertise of a global network.

International Network
OraNet includes over 100 investigative ophthalmic sites experienced in conducting clinical trials within their area of expertise.
Ophthalmalic Expertise
Experienced across the fields of Ophthalmology, Including ocular surface diseases, glaucoma, cataract and vitreo-retinal diseases.
Experienced Investigators
OraNet sites are trained and supported By Ora’s in-house clinical trial specialists to ensure protocol adherence and accelerated timelines.
Exclusive Access
OraNet sites use Ora’s validated clinical models and scales to better assess critical endpoints.

At Ora, your ophthalmic clinical research is backed by OraNet – an international network of over 100 investigative sites. Comprised of ophthalmologists across all specialties, OraNet sites are experienced in conducting clinical trials within their area of expertise, such as allergy, anti-infectives, anti-inflammatories, cataract and refractive surgery, diabetic retinopathy, diagnostic drugs and devices, dry eye, glaucoma, uveitis, wet and dry age-related macular degeneration (AMD), and many orphan diseases.

Ora consistently seeks out ophthalmologists throughout a broad geographic area to meet the diverse demands of our clients’ global research studies. Sites under consideration for OraNet undergo our highly selective evaluation process that grades the experience, skill sets, integrity, and organizational abilities of ophthalmologists and their staff.

OraNet sites are extensively trained and supported by our in-house clinical trial specialists, who work closely with each site to instruct investigators and staff before the start of each new protocol, and during the study to manage efficient trial execution and ensure protocol adherence. Exclusive access to Ora’s validated and verified clinical models and scales standardizes study environments at OraNet sites, reducing variability between sites and delivering more reliable clinical trial outcomes.

Whether your clinical research programs are in the anterior or posterior segment of the eye, OraNet has the medical expertise and clinical trial experience to deliver superior research data.

OraNet Patient Recruitment

Ora further supports OraNet sites by providing strategies and tools to properly identify the desired patient population. During study start-up, global patient recruitment strategies are developed and implemented at each site. Strategies are customized based on a site’s individual environment and the support needed to be successful in meeting project timelines. In addition, OraNet sites have exclusive access to our in-house team of seasoned patient recruiters, who collaborate with our investigative sites to generate patient databases targeted to the study population, write and train sites on the use of patient screening scripts, and performs patient recruitment on behalf of OraNET sites. Ora’s site specific strategies work to ensure that the proper patient populations are enrolled and study timelines are optimized.