In the News

The PPD clinical research business has been selected to start a Phase II clinical trial to investigate.

The authors outline how a functional service provider team implementing data standards within a global library can help to ensure the on-time delivery of clinical trials, while maintaining data quality and integrity.

Samantha Hadfield comments on ways to streamline and expedite onboarding for FSP engagements.

The authors document two early-stage challenges that exist in the design and implementation of eDiaries.

Sanra Orset reviews trends in audit findings specific to DCTs and provides guidance on how to develop a new project delivery framework that will support audit readiness.

OSP was delighted to speak to Galina Nesterova, executive medical director at the Rare Disease & Pediatrics Center of Excellence, and Susan McCune, vice president of pediatrics and clinical pharmacology both within medical science and strategy at PPD, part of Thermo Fisher. They answered some pertinent questions surrounding rare diseases.

Paul Gillard provides an overview of vaccine mega-trials conducted over the last 20 years.

Lauren Herring discusses the comprehensive and robust centralized and one-to-one patient support that characterizes patient concierge services.

Lloryn Hubbard discusses how life science companies can address the disparities within clinical trials and health equity.