Newsletter | March 14, 2023

03.14.23 -- How Sanofi Is Using Digital Devices To Improve The Patient Experience

 
     
 
     
 
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The Five Steps To User Adoption Of eRegulatory In Clinical Trials
 

For most sites, the barriers to adding new technology to their operations are not implementation related. The challenges lie in motivating user adoption of the solution. We've developed best practices for clinical trial organizations to use when moving their team from traditional paper and fragmented technology workflows to a fully electronic and purpose-built eRegulatory platform.

 
 
 
 
 
 
     
 
Clinical Trial Technology
     
Sanofi And Digital Devices: Improving The Patient Experience
 
 
In October 2022, Clinical Leader’s chief editor, Ed Miseta, interviewed Victoria DiBiaso, global head, patient informed development and health value translation, and Terttu Haring, head, clinical innovation office at Sanofi. They discussed the new R&D model, the company’s attempts to make its trials more patient-centric, and how digital technologies and devices are helping to create a better trial experience for patients. In this segment, Haring discusses how the company is incorporating digital devices to improve the patient experience.
 
 
 
 
     
A Unified Approach To Clinical Trials
 
 

Learn how developing a unified solution can improve quality and create efficiency and cost savings for organizations of all sizes conducting clinical trials of all types.

 
     
Automate The Protocol With eSource
 
 

Often hiding in plain sight in the clinical research industry, discover how eSource presents a huge and ready-made opportunity for sponsors to conduct clinical trials more efficiently.

 
     
Econsent Readiness In 12 Countries
 
 

eConsent is imperative for continuing research during the COVID-19 pandemic, but regulations can vary widely across borders. Witness how eConsent is managed in the top countries in clinical research.

 
     
Gradually Investing In Direct Data Capture Is Inevitable
 
 

Given the decentralization of clinical trials and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”

 
     
How To Deliver Highly Engaging Informed Consent For Better Study Outcomes
 
 

Master protocol design trials require an endless stream of consent forms, which add time, cost, and risk. A feature-rich electronic consent platform can simplify those processes and improve patient engagement.

 
     
A New Reality For Modern Day Research
 
 

Discover how sponsors are turning to innovative solutions that deliver electronic health records to electronic data capture integration to automate documentation and improve site relationships.

 
     
Streamline Clinical Research With TrialMaster
 
 

Organizations conducting clinical research can streamline collection, processing, and submission of clinical trial data to regulatory authorities to expedite development and approval.

 
     
Patient First Solutions For Oncology
 
 

Medable Inc's new oncology offering is an end-to-end suite that includes an extensive eCOA library, pre-built and validated DCT applications such as Total Consent and Televisit, and protocol design consulting.

 
     
IRT And eClinical Technology Considerations For Cell And Gene Therapy
 
 
Don't try to fit cell and gene therapy studies — or any kind of study — into predefined functionality. The Cenduit IRT and Quantum Interactive™ agile design platforms and reporting tools support clients’ most complex requirements.
 
     
Own, Access, And Leverage All Your Operational Data
 
 

Discover how elluminate® CTMS Insights keeps trial operations data in one place without the burden of traditional clinical trial management systems.

 
     
     
 
Choose Your Own Adventure
 
 

You're receiving the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial Technology. To make changes to your newsletter selections, update your topic preferences.

  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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