Now more than ever, life sciences organizations are under a microscope to accelerate key Clinical R&D processes. But, taking traditional in-person workflows like document verifications or clinical site monitoring digital can be challenging. Your organization needs a seamless secure way to access, verify, and share source or patient documents alike without in-person clinical site visits. 

On October 13th, 2020 FierceBiotech is teaming up with Box to discuss how your life sciences organization can continue to propel therapies & devices through the value chain with faster and even more secure site monitoring and auditing. We will discuss how to: 
  • Accelerate the verification process of documents and patient records at clinical sites with cloud technologies, like Box
  • Increase control of your clinical sites and reduce margin of error with real time access to regulated and non-regulated content 
  • Boost productivity while ensuring GxP compliance on regulated and non-regulated content 

Featured Speakers

Manu Vohra

Managing Director, Global Life Science
Box

Manu Vohra is the Global lead for Life Sciences and Go-To-Market strategy for Cloud Content Management at Box. After 2 decades of deploying ECM solutions in a regulated industry, I'm spending my efforts supporting Life Sciences companies to ride the Digital Transformation wave and fully leverage the micro content service offerings of a modern Content Platform at Box.

Kate Calkins

Solutions Engineer
Box

Kate Calkins is a Solutions Engineer at Box. In her six years at Box she has specialized in working with customers in regulated industries (including Life Sciences) from both a Solutions Engineering perspective as well as from a Customer Success lens.

Date:  Tuesday, October 13, 2020
Time:  2pm ET / 11am PT
Duration:  1 Hour

Register now for this webinar