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DIA Annual Meeting 2018 - Boston, MA

June 24, 2018 - 1:00am (EDT) to June 28, 2018 - 1:00am (EDT)

 

Bioclinica looks forward to another tremendous DIA event! Plan now to meet face-to-face in booth #1119 with Bioclinica experts from across all of our rapidly growing services including: Cardiac Safety, Clinical Adjudication, Clinical Trial Management System, Electronic Data Capture, Medical Imaging, Site Payments, Pharmacovigilance, Randomization & Trial Supply Management and Site Network. We look forward to seeing everyone in Boston.

 

Meet one-on-one with the Bioclinica experts.

Schedule a Meeting

 


Session Date and Time: Tuesday, June 26 • 1:10pm – 1:55pm

Title: Transformational Trends in Investigator Site Payments 2018

Speaker: Meghan Harrington, VP and Head of Payments & Forecasting, Bioclinica

Bioclinica Innovation Theater | Location: Theater 1

Bioclinica will present key findings from 2018 industry market research highlighting trends in investigator site payments site payments, operational efficiencies and technology adoption. Learn if a shift in outsourcing of site payments is on the horizon, plus hear industry perspectives on financial operational objectives and the impact on site relationships.

 

Session Date and Time: Wednesday, June 27 • 10:30am - 11:45am

Title: Clinical Data: Let's Get to the Source and Streamline it to the End

Chair: Jennifer Price, Senior Director, Clinical Data Management, Paidion Research

eSource is simply the use of the original source data as collected, without requiring transcription. In this session with Jennifer Price, Bioclinica's thought leadership of eSource solutions will be spotlighted, as the session presents successful implementations, case studies, challenges, activities, and best practices by leading industry pioneers.

 

Session Date and Time: Wednesday, June 27 • 4:00pm - 5:15pm

Title: Design and Statistical Considerations for Real-World Evidence to Support Regulatory Decision Making

Speaker: Ankit Pahwa, MS, Manager, Biostatistics, Bioclinica

Real-World Evidence in Regulatory Decision Making

Regulators expect drug makers to conduct novel studies to provide treatment effectiveness results that are valid in everyday clinical practice. This session will present opportunities and challenges in pragmatic trials to generate real-world insights.

 

Dr. Joby John

Session Date and Time: Thursday, June 28 • 9:00am - 10:15am

Title: Improving Efficiency and Effectiveness in Data Management of Pediatric, Rare Disease, and Oncology Trials

Chair: Joby John, Senior Director, eHealth Operations, Bioclinica

Guest Speaker: Joe Anderson, Senior Consultant, Paidion

Technology in Data Management of Pediatric, Rare Disease, and Oncology Trials

This session will present case studies, best practices, and technology interventions that have helped sponsors, CRO's, FSP's and technology companies in improving efficiency and effectiveness in clinical data management of pediatric, rare disease, and oncology trials.

 

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Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

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