Device Assessment
The development of ophthalmic medical devices requires expertise in ocular surgical procedures, a deep understanding of critical endpoints, and the ability to address challenges during preclinical ophthalmic device evaluation.
As a specialized non-GLP ophthalmology CRO, Powered Research brings over 10 years of experience in assessing the safety, tolerability, and efficacy of ocular devices, helping accelerate translational development and clinical readiness.
Our Medical Device Expertise Includes:
-
In-situ intraocular pressure measurement devices
-
Glaucoma shunts
-
Intraocular lenses
-
Subretinal devices
Types of Studies We Conduct:
-
Early biocompatibility studies
-
Ocular tolerability assessments
-
Efficacy evaluations in established and custom animal models
-
Acute and chronic studies
Our Services
Powered Research is well known for rapid study turnaround, and our scientific experts allow for timely study scheduling and execution.
Our staff has extensive expertise in the design and development of non-GLP preclinical data packages, including tolerability and pharmacology models, drug distribution studies, and custom experimental designs.
AAALAC Accredited
Certified Excellence
Flexibility
Use our internal protocols or work with us to design your own.
Scalability
Our clients include small startups, large pharma companies, and biotech companies.
70 Domain Experts
A committed team of scientists, veterinarians, and technicians.
Satisfaction
97% of our clients place a second study with us in the first 6 months.
​
