OUR SERVICES
HOSPITALS & PRIVATE PRACTICES
- Synergistic Approach: Facilitate a symbiotic partnership between Physician Investigators and Pharmaceutical Sponsors
- Patient Community: Empower your patients to enhance their overall lives, extending the impact of healthcare beyond treatment and fostering a sense of well-being
- Growth Advance: Additional source of physician referral, academic breadth, and marketing
- Financial Advantages: Optimize leverage and execution of favorable revenue fees
- Recognized Gains: Assertively manage trial patient billing
- Deliverables: Punctual execution and adept trial management ensure regulatory compliance and strategically yield cost savings
- Strategic ROI: Diminish operating costs associated with site-level research activities
BIOPHARMA INDUSTRY
- Exclusive Multi-Site Network: Access top investigators across multiple sites for widespread trial impact.
- Rapid Study Start-Up: Streamlined initiation ensures minimal delays and faster study commencement.
- Precise Data Delivery: Punctual, accurate data empowers informed decision-making.
- High Patient Accrual: Accelerated recruitment from a diverse participant pool.
- Prequalified Site Efficiency: Expedite studies with prequalified sites, reducing administrative burdens.
- Integrated Technology Tools: Seamlessly integrate cutting-edge tools for enhanced data management.
- Patient Matching Database: Access a comprehensive network-wide database for targeted participant identification.
- On-Site Professional Staffing: Ensure optimal study execution with dedicated on-site professionals.
GROWTH & REVENUE
- Seamless and Proficient Management of Trial Patient Billing Processes
- Punctual Execution and Strategic Trial Management Resulting in Significant Cost Savings for Clients
- Substantial Reduction of Operational Costs Through Efficient Management of Research Activities at the Site Level
- Implementation of Advanced Financial Strategies for Budgetary Optimization
- Continuous Evaluation and Adaptation of Financial Strategies for Ongoing Operational Excellence
QUALITY & DELIVERABLES
- Investigators and site selection based on clinical expertise and adherence to ICH Good Clinical Practice (GCP) and FDA CFR guidelines.
- Robust internal audit process ensuring high-quality data.
- Rigorous Monitoring and Oversight Ensuring Fiscal Efficiency Throughout the Trial Lifecycle
- Stringent data integrity oversight, influencing repeat site selection.
- Streamlined processes for investigators, alleviating staff burden and facilitating optimal trial performance.
© 2021