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Infrastructure Design: Key to Enhanced Clinical Trials Data Management

PPD Laboratories experts on PPD's central lab data management service and how it can mitigate challenges throughout a trial.

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Natural History Studies in Rare Diseases and Genetic Biomarkers

By Andrew Bevan, director, project management, peri- and post-approval operations, Evidera; Moira Ringo, senior consultant, real-world evidence, Evidera; Leona C. Fitzgerald, senior director, regulatory affairs, PPD; Fiona Kearney, senior director, project management, peri- and post-approval operations, Evidera; and Delphine Saragoussi, research scientist, real-world evidence, Evidera.

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Patient Engagement in Clinical Trial Protocol Design and Recruitment Strategies

Kevin Marsh, executive director, commercial strategy and new product development, patient-centered research, Evidera, and Margaret Vernon, vice president, general manager, patient-centered research, Evidera, discuss trial design and strategies for success.

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Outsourcing from a Pharmacovigilance Perspective

Tina Bostic, executive director, pharmacovigilance, discusses PPD’s outsourcing strategy through expanding the global labor force.

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Putting Patients First Through Data-Driven Solutions

Gaurav Bhatnagar, VP strategic feasibility, site and patient access, talks data-driven solutions and how they help us focus on patients.

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Randomization Feb 2019

The Do's and Don'ts of Randomization in Clinical Trials

Jolee Graham, biostatistics director, Nicki Payne, director, IRT, and Katy Tam, director, biostatistics, discuss the components of successful randomization in research.

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The Benefits of Glucose Clamp Procedures in Clinical Trials

Adalberto Barba Jr., director of clinical operations, early development, at PPD’s clinical pharmacology unit in Las Vegas, Nevada, discusses the site’s capabilities in glucose clamp studies.

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Our Enrollment Solutions: PatientAdvantage

A new way of thinking about clinical development and delivery

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Balancing Scientific Value and Identification Risk in Anonymization

An overview of anonymization strategy for clinical documents in response to EMA Policy 0043 and Policy 0070

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Combining FSP and FSO Outsourcing Strategies

By Dave Agrella, vice president, functional service partnerships (FSP) and Timothy King, DrPH, executive director, FSP.

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