It’s about time you were provided with a site and process customized to meet your every need from rapid site identification and initiation to timely recruitment of patients. We are ready to meet your study needs when you are – today.
- Quick feasibility assessment and feedback
- Rapid site identification and recommendation
- Prompt, ‘right first time’ document completion – centrally coordinated
- Quick contract negotiation and completion – one contract, one budget
- Central ethics
- Timely patient recruitment and enrollment
It’s all about the data. Delivering good quality data and protecting study integrity is our focus every step of the way. We ensure this with our rigorous training and quality support program.
- GCP-trained investigators and coordinators
- Active, ongoing SOP training
- Sponsorship of CCRP accreditation
- GCP training aids and newsletters
- Continuous quality support and performance review
Our results say it all: Our sites routinely surpass enrollment expectations and we perform exceptionally well in key trial metrics including screen-failure rates and subject completion rates. We have built our reputation on our results and our clients choose us again and again.
- Routinely surpass enrollment targets
- Minimized screen-failure rates
- Excellent patient compliance and retention
- Central enrollment strategies and initiatives
- Centralized and site-specific advertising and media creation, placement and metrics
- Experienced in hundreds of Phase II-IV trials in multiple therapeutic areas