Early Phase CRO Solutions
DVCR’s clinical trial services as a contract research organization (CRO) include project management, data management, biostatistics, statistical programming, PK/PD analysis, medical writing, clinical and medical monitoring as well as site feasibility and management for multi-site trials with our global network of site partners. Additionally, DVCR operates one of the most innovative and technologically advanced clinical pharmacology units in the world with over 90 beds for overnight confinement for phase I studies, a cGMP compliant pharmacy as well as luxurious amenities to support diverse study participant recruitment and retention. By leveraging technology and one of the country’s most experienced leadership teams in early phase clinical trials, DVCR provides Smarter Faster Data® to its biopharmaceutical clients.
Multi-Site Trials
Data Management
PK/PD Analysis
90-Bed Phase I Unit
Biostatistics
Medical Monitoring
Project Management
Medical Writing
Clinical Monitoring
Early Phase CRO Solutions
DVCR’s clinical trial services as a contract research organization (CRO) include project management, data management, biostatistics, statistical programming, PK/PD analysis, medical writing, clinical and medical monitoring as well as site feasibility and management for multi-site trials with our global network of site partners. Additionally, DVCR operates one of the most innovative and technologically advanced clinical pharmacology units in the world with over 90 beds for overnight confinement for phase I studies, a cGMP compliant pharmacy as well as luxurious amenities to support diverse study participant recruitment and retention. By leveraging technology and one of the country’s most experienced leadership teams in early phase clinical trials, DVCR provides Smarter Faster Data® to its biopharmaceutical clients.
Multi-Site Trials
90-Bed Phase I Unit
Project Management
Data Management
Biostatistics
Medical Writing
PK/PD Analysis
Medical Monitoring
Clinical Monitoring
Multi-Site Trials
90-Bed Phase I Unit
Project Management
Data Management
Biostatistics
Medical Writing
PK/PD Analysis
Medical Monitoring
Clinical Monitoring
WEBINAR ON-DEMAND
Definitive QT Evaluation – Clinical and Operational Considerations
Discover strategies to optimize QT assessments for successful regulatory submission outcomes. Our expert-led session will explore pathways for regulatory waiver of a standalone TQT, submission deliverables and data collection best practices.
WEBINAR ON-DEMAND
Definitive QT Evaluation – Clinical and Operational Considerations
Discover strategies to optimize QT assessments for successful regulatory submission outcomes. Our expert-led session will explore pathways for regulatory waiver of a standalone TQT, submission deliverables and data collection best practices.
WEBINAR ON-DEMAND
Definitive QT Evaluation – Clinical and Operational Considerations
Our Multi-Site Model
By combining our robust CRO support services and a global network of strategic site partners, Dr. Vince Clinical Research (DVCR) can now manage multi-site Phase I-II studies in patients, specialty populations and healthy normal volunteers across a diverse range of therapeutic areas and trial designs.
Our model prioritizes sites that leverage these principles to help our sponsors reach their milestones faster.
Site ID and Selection
Quality over quantity is imperative for a successful model as we are not trying to be all things to everyone.
Prioritizing Site Payments
Sites need quicker payments to avoid study delays. This reinforces our collaborative, true partnership approach.
Site Engagement
We are committed to being a true partner, providing sites with essential tools, support, and prioritizing transparent communication and collaboration.
Lead Site ModelTM
DVCR as Lead Site expedites recruitment, mitigates issues, standardizes conduct and data, and provides hands-on training for sites.
Our Multi-Site Model
By combining our robust CRO support services and a network of over 50 strategic site partners across North America, Dr. Vince Clinical Research (DVCR) can now manage multi-site Phase I-III studies in patients, specialty populations and healthy normal volunteers across a diverse range of therapeutic areas and trial designs.
Our model prioritizes sites that leverage these principles to help our sponsors reach their milestones faster.
Site ID and Selection
Quality over quantity is imperative for a successful model as we are not trying to be all things to everyone.
Prioritizing Site Payments
Sites need quicker payments to avoid study delays. This reinforces our collaborative, true partnership approach.
Site Engagement
We are committed to being a true partner, providing sites with essential tools, support, and prioritizing transparent communication and collaboration.
Lead Site ModelTM
DVCR as Lead Site expedites recruitment, mitigates issues, standardizes conduct and data, and provides hands-on training for sites.
Every single detail of DVCR and our Phase I unit has been reimagined to provide the optimal environment for clinical study execution
