For sponsors & CROs
A site that delivers clean data on schedule
Experienced investigators, a bilingual recruitment engine, and documentation your monitors can rely on.
Why sponsors place protocols with us
Our site combines an established community recruitment base with disciplined source documentation and responsive communication with monitors and study managers.
- Bilingual staff and consent materials expand the eligible population
- Dedicated regulatory support for IRB submissions and essential documents
- Same-week feasibility responses for protocols in our therapeutic areas
- Monitor workspace and prepared source available for scheduled visits
Therapeutic experience
Cardiology, diabetes and endocrinology, neurology, dermatology, vaccines and infectious disease, and women's health. Detailed site experience summaries and investigator CVs are available on request.
Working together
Feasibility questionnaires, site qualification visits, and contract and budget discussions are handled by a single point of contact so timelines stay predictable.
Frequently asked questions
Answers to questions we hear most often.
What therapeutic areas does Salud specialize in?
Cardiology, diabetes and endocrinology, neurology, dermatology, vaccines and infectious disease, and women's health. We review protocols in adjacent areas case by case.
How quickly can you respond to a feasibility questionnaire?
For protocols in our core areas we typically return completed feasibility within the same week of receipt.
What recruitment resources do you maintain?
We maintain a consented recruitment database, community outreach relationships, and bilingual outreach materials. Current database figures are shared during feasibility.
Are you GCP and FDA compliant?
Yes. Staff complete documented GCP training, and studies are conducted in accordance with applicable FDA regulations and the approved protocol under IRB oversight.
How do you handle monitoring visits?
We provide dedicated monitor workspace, prepare source in advance of scheduled visits, and respond to queries within agreed timelines.
Evaluating sites for an upcoming protocol?
Send us a synopsis and we will return feasibility promptly.
Partner with usInformation on this website is provided for general educational purposes about clinical research and is not medical advice. Participation in any study is voluntary.