CAPABILITIES
Our comprehensive approach to trials conduct is tailored to Sponsor and Participant needs.
Eximia Research’s multidisciplinary team can support the full range of clinical trial requirements: from feasibility studies (inclusive of the expert Investigator opinion and feedback on protocol design) and expedited study start up to accelerated subject enrollment coupled with the highest integrity of trial conduct.
Eximia Research is a fully integrated clinical site network that leverages centralized platform services support to deliver quality data within our research clinics.
From feasibility and site selection process, a rapid site start-up and signing a single contract/budget to access all our sites, our centralized platform support team focuses on expedited and highly efficient processes to help Sponsors save time and money.
The staff at Eximia Clinical Research has certified, experienced and dedicated GCP-trained physicians / clinical investigators and research personnel, including:
- Board-Certified Physicians
- Physician Assistants
- Nurse Practitioners
- Full-time Clinical Research Coordinators
- Trained Research Assistants
- Quality Assurance Team
- Regulatory and Start-up Specialists
- Data Entry Personnel
- Patient Engagement and Recruitment Specialists
- Marketing and Advertising Team
- Business Development Team
- CTMS and Other Research Technologies Admin
- Finance Team
- Human Resources and Talent Acquisition
This mix of dedication, ethics and expertiseis what makes Eximia Research stand outin the clinical research industry.
A centralized platform Research Network
Areas of Expertise
Site Start-up and Feasibility Team
Marketing and Community Outreach
Training and education
Technology and Innovation
Patient Engagement and Recruitment
Finance and Contracts / Budgets Team
Quality Assurance program
Project Management / Regulatory Team
✅ Experience
✅ Excellence
✅ Exceptional Results
Our facilities are equipped with the latest and most advanced testing, research and diagnostic equipment.
Our state-of-the-art resources include:
- Fibroscans
- Access to Certified Endoscopy Unit (colonoscopy, upper endoscopy, sigmoidoscopy and liver biopsies)
- Access to Gastrointestinal lab (24-hour/pH monitoring) with smartcam capsule
- On Site CLIA waived diagnostic laboratory
- Radiology with access to: bone densitometer, CT scanner, MRI,PET and ultrasound units
- Cardiovascular testing: heart station, including EKGs, echocardiograms, treadmills, holter monitoring and ambulatory blood pressure monitoring
- Spirometry
- Certified digital mammography unit
- Secured investigational drug storage facilities with electronic key access and video monitoring
- Sleep lab (EEG, polysomnography studies and MSLT’s)
- Weight Management and Nutrition Center
- Infusion and pharmocokinetic monitoring capabilities
- Monitoring suite with wireless internet and high speed modems, telephone lines, as well as fax and copier machines
- Drug testing
- Temperature and humidity-controlled, secured pharmacy, including back-up air conditioning system connected to a power generator
- Double-lock refrigerators, freezers (-20°C, -70°C, and -100°C)
- Continuous temperature monitoring of drug storage area and refrigerated unit with alert system
- Laminar fume hood and sterile drug preparation area
- Point-of-care testing
Technologies:
- eConsent capabilities
- Decentralized and virtual capabilities
- eRegulatory management
- CTMS platform via Clinical Conductor
- Firewalls in place to ensure safe and secure internet connectivity
- Part 11 Compliant
- Multi-factor authentication and other measures to ensure information security
- LMS for employee training
- Secure servers (including 24/7 surveillance and bio-metric access)
- Secure Socket Layer (SSL) data encryption
- Wireless internet access
- Stipend payments through ClinCard