Advancing Medical Science with HexisHealth technology
Cutting-Edge Technology
Our groundbreaking HIPAA compliant "e-ligible" system is a cutting-edge, first of kind and the only clinical trial enrollment technology that revolutionizes the patient recruitment process.
Designed to enhance efficiency and ensure compliance, this innovative solution is custom made to seamlessly integrates with your Study Protocol eligibility criteria to enroll only eligible patients into your clinical trials, eliminating statistical, practical and ethical implications and mis-randomizations with no involvement of AI.
About Us
Experience and Difference
Experience and Difference
Experience and Difference
At Hexis Health, we work with pharmaceutical companies, biotechnology companies, clinical research sites, contract research organizations (CROs), and others to enable those organizations to deliver their research in a time-efficient manner in compliance with GCP, FDA and State specific Regulations.
How We Help
Experience and Difference
Experience and Difference
Hexis Health delivers operational and administrative support services to the clinical research companies. This includes everything from handling regulatory and compliance activities to managing patient recruitment staffing and data collection. We also provide support with study start-up, monitoring, and closeout.
Why Hexis Health
Experience and Difference
Why Hexis Health
Dedicated to Quality,
At Hexis Health, we strive to provide our clients with the highest level of expertise.
Our team of highly skilled and experienced professionals are proudly committed to providing and conducting clinical trial support for our clients.
Our Services
Site Management Services
HexisHealth Site Management Department is full service,
We employ and train our regulatory & clinical coordinator staff to the highest industry standards and manage study contracts for our associated sites. We take on trials and provide the necessary oversight.
We also provide consulting services such as business development, clinical operations, contracts and budgets.
Training & Support
On-Boarding Programs as well as On-Site Training & Support for Site, CRO & Sponsor staff including:
- Regulatory Department,
- Study Coordinators (SCs),
- Clinical Research Associates (CRAs),
- Clinical Research Coordinators (CRCs),
With accredited Course Certificate of Completion.