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Program Coordinating Center

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

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Conducting post-approval research requires a unique mindset and specialized infrastructure. Do you have what it takes?


Patient Centric Post-Approval Research: It's Time to Rethink How Post-Approval Studies Are Done


Maximize the ROI of Your Post-Approval Research

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Post-Approval Research

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Patient Outreach Center

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Program Coordinating Center

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Post-Marketing Research

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Leader in Clinical Trial
Management Solutions

Bioclinica is divided into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging and Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Biomarker Laboratory. Our eHealth segment comprises an eClinical Solutions Division along with Safety and Regulatory Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

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