FOR HOSPITALS, ORGANIZATIONS, PRIVATE PRACTICES
- Deployment of our Ease-Of-Use model for trial management and gap analysis
- Access to professional trial management staff
- Commission Accreditation assistance (COC, CCC, Joint Commission)
- Strategies for the efficient integration of clinical research into the healthcare workflow
- Access to cutting-edge treatment options and Sponsor trials
- Additional sources of physician referral, academic breadth, and marketing
- Current study protocol, recruitment and financial expertise
- Options to diversified revenue source
FOR SPONSORS
- Exclusive multi-site network and PI access
- Rapid study start-up model (2-8 weeks depending on the study)
- QC data delivery
- Thorough database of site profile
- Ease of study start-up of prequalified sites
- Comprehensive, on-going programs including project management, financial management, education and training
- Network-wide patient matching database access
- On-site professional staffing for optimal study success
QUALITY AND OUTPUT
- Investigators and sites selection based on clinical expertise and ability to perform within ICH Good Clinical Practice (GCP) and FDA CFR guidelines
- Strong internal audit process, ensuring high quality data
- High data integrity oversight for repeat site selection
- Ease of burden on Investigator staff
GROWTH & REVENUE
- Collaboration of Physician Investigators and Pharmaceutical Sponsors
- Standardized budget process
- Provide leverage and faster execution of contract negotiations
- Cost Management
- Timely execution and effective trial management brings cost savings to our clients
- Decrease operating costs to manage research activities at the site level
