What We Do
Nosara is a full-service CRO offering clinical trial and research services. We provide superior monitoring and detailed results to numerous pharmaceutical and device companies worldwide.
“We are a global CRO working with sponsor companies from around the world to facilitate approval of your pharmaceutical and medical devices. What we do is an enormous responsibility and, in many ways, we are the next step in bringing products to the global healthcare marketplace which can improve the lives of billions of people. What we do at Nosara is incredibly important and are honored to work with the best research teams and medically innovative companies in the world.”
--Jill Emerton, Founder and CEO of Nosara Clinical Consulting, LLC
From proof of concept to post-market studies,
Nosara has unrivaled experience with clinical trials in Latin America
Ophthalmic Research
- Cataract
- Glaucoma
- Dry eye
- Cell therapy
- Laser/refractive
- Cornea
Other Areas of Research
- Dermatology
- Oncology
- Diabetes
- Cardiology
- Urology
- Infectious disease/vaccines
- Neurology
- Rheumatology
- Rare diseases
Clinical Operations
- Project Management
- Monitoring
- Protocol Development
- Data Management
- Medical Writing
- Certified Spanish translations of all study documents as required by local regulatory bodies
Regulatory and Auditing
- Site preparation for regulatory inspections
- Liaison between sponsor and regulatory bodies
- Country-specific submissions
- Safety reporting
At Nosara, we are dedicated careful data collection, precise research, and sound consulting advice.
We offer study support from A to Z, providing exceptional project management services to our clients, investigators, and partners. This includes a full range of clinical operations, from clinical trial management to site selection and study execution. As a global business, Nosara relies on experienced, local resources with extensive knowledge of the country-specific regulations. By doing so, Nosara is very familiar with the requirements necessary to carry out an efficient and successful trial anywhere in the world.
Throughout the clinical planning phase of your trial, the Nosara medical services team is there to help advise pharmaceutical and biotechnology companies. Our qualified team of experts is hyper-focused on subject safety and have a proven track record of CRO service delivery. At Nosara, we are diligent about conducting research with the highest of ethics and integrity. We are committed to delivering high-quality statistics and are staffed with an internationally respected, experienced team of published medical writing professionals known for clinical, regulatory, and scientific papers. Our relationships with industry leaders, partners, and vendors allow us to ensure that the trials we manage are accurate and concise from the concept phase through approval.