Post-approval studies are complex and composed of many moving parts. Without careful planning and administration, your study will experience costly delays and inefficiencies. At Bioclinica, we entrust the management of post-approval studies to our Program Coordinating Center (PCC). Our global PCC staff is 100% dedicated and are experts in the details of conducting post-approval research successfully.
Exclusively Focused on Coordinating and Supporting Participating Sites
Our PCC is designed to assist research sites around the globe by decreasing administrative burden and providing excellent customer service throughout the course of your post-approval study. With the power of our PCC behind your post-approval study, you benefit from:
- Validated SOPs developed expressly for post-approval studies
- Staff located globally to ensure real-time support in local languages
- Execution of site management strategies tailored to meet the needs of physicians, from seasoned clinical research sites to research-naïve physicians
- Remote monitoring that leverages post-approval-specific technology to enhance engagement and compliance with established protocols throughout the course of the study
- Customized study reports that integrate multiple discrete data sets to help you analyze data and gain clarity