Cognizant

http://www.appliedclinicaltrialsonline.com/act_w/pathway

Sites are challenged with exchanging documents with sponsors throughout the life cycle of a study, and those with a technology gap often rely on cumbersome manual processes that involve email and paper. Join this webinar to find out how the preeminent investigator platform deeply integrated with the leading eISF solution automates the flow of documents connecting to sponsor eTMF systems, enhancing site-sponsor collaboration, compounding efficiencies and accelerating trials.

Learn how to expedite your studies by enabling end-to-end document exchange between sponsor eTMF systems and the Florence eRegulatory solution through Cognizant SIP’s eISF Connect Module.

Discover how to boost site satisfaction to become the sponsor of choice by providing your sites with Florence’s leading eISF in use by over 8,500 research teams.

Find out how to help modernize your sites at scale by migrating from paper-based binder processes to digital, virtual collaboration with automated workflows and eSignature capabilities.

: Larissa Comis, Product Lead, Shared Investigator Platform, Cognizant

Vishal Janani, Associate Director, Cognizant Life Sciences

: Thursday, June 17, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

On demand available after final airing until Jun. 17, 2022.

Webcasts

*** Thursday, June 17, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Join this webinar to hear best practices on how to enhance site-sponsor collaboration, compound efficiencies and accelerate trials by enabling end-to-end document exchange between sponsor eTMF systems and Florence’s leading eISF solution through Cognizant SIP.    ***On demand available after final airing until June 17, 2022***

Creating an Integrated Digital Pathway for Sites and Sponsors

http://www.appliedclinicaltrialsonline.com/act_w/clinical_platforms

Site-centric clinical platforms deliver greater operational efficiencies and accelerated timelines across clinical trials. Discover how 7 of the top 15 global biopharmaceutical companies came together on a single clinical technology platform and operate through common workflows and leverage common trial documents. In turn, find out how this environment helps sites and investigators stay at the center of this ecosystem.

Hear about site and sponsor experiences and how they have leveraged the cloud-based solution in addition to what efficiencies they’ve discovered

Identify how harmonized management of key components of clinical trials across industry stakeholders can improve clinical trial timelines

Identify how to facilitate sponsor and site collaboration on key clinical trial documents, enabling seamless workflow and document exchange between site and sponsor TMF systems reducing the burden on both study teams and sites


Larissa Comis, Product Lead, Shared Investigator Platform,Cognizant Life Siences

Dr. Lestter Cruz Serrano, Medical Affairs Advisor,Cognizant Life Sciences

Hobs Apell, Senior Executive Director, Clinical Trials Office, KUCC

Wednesday, Aug. 26, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

	On demand available after airing until Aug. 26, 2021.

Come listen to how peers were able to improve site performance by consolidating access to different clinical technologies. Join us during a webcast to discuss how to alleviate your sites’ operational inefficiencies and administrative challenges via a centralized platform. 

Live: Wednesday, Aug. 26, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

On demand available after airing until Aug. 26, 2021.

Cognizant

Articles

Creating an Integrated Digital Pathway for Sites and Sponsors

Site-Centric Clinical Platforms Are Better for Sponsors