As the world leader in ophthalmic clinical trials, Ora provides a complete range of development services, including drug, drug delivery, medical devices, and preclinical. Over the past 30 years, Ora has earned 34 regulation product approvals for our clients. Our validated, industry standard models and established methodologies are paving the way for future regulatory approvals, both in the US and around the world.
Global
Unequaled Ophthalmic Experience – 30 years, 34 product approvals
R&D
Ora has been on the cutting edge of ophthalmic product development expertise for over 30 years
Expertise
Find out how our knowledgeable staff and strict protocol adherence can help you accelerate your development timelines.
Consulting
Ora is able to offer truly unique consulting value across all ophthalmic therapeutic areas.
Formulation
We help your company quickly and efficiently advance your drug candidates to the next stage.
Preclinical
A full range of preclinical models in Dry Eye, Ocular Allergy, AMD, and Diabetic Retinopathy.
Clinical
We design, execute, and innovate the most efficient ophthalmic clinical development programs in the industry.
Regulatory
Our Regulatory Writing Team is highly accomplished in a wide array of regulatory document preparation.
Marketing
Our experienced creative professionals can provide you with all of the tools you need to succeed.
In the world of dry eye, it’s not about finding the most subjects.
It’s about finding the right subjects.
500,000 CACs and 19 FDA approvals later, the Allergy breakthroughs keep coming.
