Keeping R&D Data and Regulatory Approval Processes Advancing in Alignment

DIA & Salesforce White Paper
This white paper is part of DIA’s White Paper Library
In an era of expiring patents, spiraling costs, and increasing competition, effective therapies must be developed more quickly and efficiently than ever. This white paper examines how pharmaceutical  and other life sciences organizations can keep critical data, R&D, and regulatory approval processes advancing in alignment.

By utilizing new cloud-based and mobile first technologies, artificial intelligence, and other modern tools, you can:
  • Connect teams to speed up trial enrollment, increase patient engagement, and improve the patient experience.
  • Deploy secure, authenticated portals that allow patients and investigators to share information and collaborate seamlessly.
  • Unify disparate systems to intelligently leverage operational data, predictive analytics, and reporting to more deeply understand each study.
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INTERESTED IN PUBLISHING?

For more information on publishing your White Paper with DIA, including schedule and pricing, please contact Heej Ko at Heej.Ko@DIAglobal.org.