One Team - One Approach
Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.
Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.
- Operations
- Regulatory Affairs
- Biometrics
- Clinical Informatics & Feasibility
- Labs
- Imaging
- Regulatory Services
- Study Start-Up
- Clinical Trial Management
- Vendor Management
- Clinical Packaging & Supplies
- Patient Recruitment & Retention
- Clinical Monitoring
- Data Management
- Biostatistics
- Medical Monitoring
- Safety & Pharmacovigilance
- Endpoint Adjudication
- Independent Data Monitoring Committee (IMDCI)
- Medical Writing
- Quality Assurance
- Account Management
- Central Labs
- Bioanalytical Labs
- Imaging Core Labs
- Cardiovascular Labs
- Phase I Unit
- Clinical Trial Management System
- Electronic Data Capture (EDC)
- ePRO / eCOA / eDiary / eConsent
- Interactive Response Technology (IRT)
- ClinTrak Data Explorer
- Centralized Monitoring
- eTMF
- Wearables
- Imaging Management
- TrialPACE Patient App
- OnPACE Site App
- Lab Information
- Management System (LIMS)
Streamline your development
We offer a full partnership instead of an “extra set of hands.” Our full breadth of services and collaborative model provide the ideal platform to execute studies at the highest level of quality.
Helping You Push the Boundaries of Clinical Research
Biotech innovation is transforming the world. In parallel, clinical development is increasingly more complex and challenging – from scientific, operational and regulatory perspectives. We help biotechs – the trailblazers of the industry – accelerate the development of their therapeutic under our full-service model that combines operational, medical, and regulatory expertise with our own wholly owned labs, imaging services, cardiac safety, and Phase I Unit, to provide our clients with one integrated solution.
Comprehensive Services and Capabilities
In the complex environment of clinical development, the more vendor partners that are involved, the higher the chance for conflicts in the drug development process. This is where our full-service model with comprehensive services streamlines the process and – Makes the Complex Seamless for our Sponsors. Competence and empowerment to coordinate all services under one roof provides an accountable, integrated, and efficient platform – increasing quality and speed while significantly reducing a Sponsor’s need for duplicate management oversight. From First-In-Human studies through late phase clinical development, we provide comprehensive services and capabilities to support your studies and programs.
Right-sized for Responsiveness
Biotechs are confronted with an ever-changing slate of top priorities. The ability to fully rely on your CRO to execute studies – almost independently – allows you to focus on other pressing issues. Being Trusted by Biotech® means that we form collaborative relationships and our teams are as invested in the science of your products as much as you are. At the same time, we are large enough to conduct complex trials globally, yet small enough to maintain a higher level of commitment.
