Healthcare

WHITE PAPERS AND CASE STUDIES

• Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC

  Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.

• How Sponsors And CROs Can Fully Benefit From The Permanent Shift To Decentralized Home-Visit Clinical Trials

  To aid sponsors and CROs in fully realizing the benefits of decentralized clinical trial methods moving forward, this whitepaper extracts the lessons learned from the pandemic and their implications for clinical trials now and in the future.

• Logistics, Transport Challenges Require Complex Solutions

  The pandemic created additional obstacles for the clinical supply chain. Ensuring continued clinical trial operation requires an optimal management solution for clinical material supply.

• The Promise Of PCM: Getting To Maturity

  PCM offers a number of advantages, including streamlined development and increased flexibility. Review the key drivers for PCM as well as the hurdles that stand in the way of industry-wide adoption.

• Empowering Freenome: Large-Scale Data Quality And Compliance

  Delve into the five key ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.

• Understanding CDMO Selections: Getting It Right

  Learn the importance of identifying CDMO key decision-makers and exploring how they reach determinations that reshape imprecise product-based marketing into messaging that addresses specific customer concerns.

• QC Lab Program And Project Management

  A client aimed to consolidate quality control laboratory operations into a singular facility and operate as one organization. Gain insight into the services that helped deliver the project on schedule.

• Regulatory Approval For Novel Device Achieved With Comprehensive Clinical Data Management

  Find out how data capture and management activities, programming, and medical writing for a clinical study report were supported to solve the major diagnostic challenge of distinguishing between bacterial and viral infections.

• How To Save 9k Hours And Cut Deviations By 27%

  This pharma company transitioned off paper, slashing their deviation count and saving thousands in onsite hours. Learn how they were able to streamline business operations and free up resources.

• Top 10 Biopharma Achieves Significant Regulatory Efficiency

  Discover how a top 10 biopharmaceutical company expanded its regulatory efficiency and automated key workflows between their IRB Platform and their electronic master file (eTMF).

• eSource Enables Speed, Flexibility, And Higher-Quality Data

  A truly integrated eSource Solution, including DDC, eCOA, and eConsent, facilitates remote or decentralized clinical trials by ingesting data from multiple sources and consolidating it into a single data set.

• Getting The Lead Out Of Flint Part 1: The Path To Data Science

  After discovering elevated levels of lead in Flint's drinking water, the city of Flint announced the FAST start program to replace the city's lead service lines.