A full-service CRO that delivers to your expectations
Regulatory, Study Start Up, and Grant Management Services
Incorporating principals of Lean Six Sigma methodology, Advanced Clinical’s strategic approach to Rapid Study Start-up begins with comprehensive feasibility and site selection. Once a site is selected a series of parallel processes within clinical operations is triggered to achieve:
- Regulatory compliance
- Fully executed budget and contract
- Delivery of investigational product (IP)/device & clinical supplies
- Comprehensive study-specific site training
Prospective and active submission planning guided by regulatory intelligence in local and global affairs ensures start-up timelines are accurate and achievable. Through collaborative engagement, Advanced Clinical drives the IRB/EC process to accelerate approvals from initial review through successful trial termination.
AC also offers regulatory consulting, product development and registration, and agency liaison services, including key sponsor support for all regulatory authority interactions.