Life Sciences Blog | Clinical Trial Solutions & Pharma IT | d-wise

Reduce Audit Risk and Submission Timelines with Accel

Written by d-wise | March 31, 2020

In this on-demand webinar, we share how to scale data volume and statistical programming users while maintaining compliance and performance with Accel.

We'll cover the following topics:

  • Outsourcing validation & compliance within GxP guidelines

  • Storage options that allow increased data variety & volumes on-demand

  • How to manage global users & system consolidation during an expansion period