Ora’s clinical operations team has a proven track record in turnkey clinical study conduct. Our approach is customized to your project needs in terms of study design, patient population, and geography.
Ora provides seamless solutions to our clients through the utilization of industry leading technologies like iMedNET, Medidata and SAS.
OraNet is a global network of 400 ophthalmic sites ready to execute your program across The Americas, Europe, Asia and Australia.
Clinical trial subject recruitment and retention is challenging. From the earliest planning stages, we will collaborate to find the appropriate population and create a retention plan to maintain subjects for the duration of the study.
Ora’s team of industry experienced ophthalmologists cover all anterior and posterior segment indications. Our medical monitors provide safety oversight and strategic clinical guidance from topical through complex routes of administration, such as sub retinal injections.
Our CRA team is strategically situated around the world to provide local geographic monitoring and confidence that studies are executed to the highest quality standards. Our CRAs have a minimum of 2 years of ophthalmology experience and as a team have one of the lowest turnover rates in the industry.
We offer manufacturing guidance and oversight of cGMP clinical supplies and packaging, labeling and depot services to maintain the highest level of quality for your clinical trial materials.
Ora’s dedicated quality team provides independent oversight and auditing to ensure the integrity of the data for every clinical study.
Complexities and regulations constantly change within the life sciences industries. Stay ahead with Ora.