Newsletter | January 3, 2023

01.03.23 -- Sanofi Builds Single Patient Data Interface

 
     
 
     
 
 
 

Welcome to the Tuesday edition of the Clinical Leader newsletter, focusing on Clinical Trial TechnologyUpdate your topic preferences to receive additional Clinical Leader newsletters on:

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

Sanofi has adopted a patient informed research and development model within the organization. The goal of the model is to work with patients, patient groups, and patient communities to understand the concerns of patients and ensure those voices are heard throughout the company. The company defines this approach as engaging with patients and caregivers, hearing their concerns, and translating those insights into actions that will help develop meaningful healthcare solutions. Learn how their single patient data interface is going to improve the lives of patients.

 
 
 
 
     
How To Deliver Highly Engaging Informed Consent For Better Outcomes
 
 

Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk to each study. A feature-rich electronic consent platform can simplify those processes and improve patient engagement along the way.

 
     
Why Research Sites Don’t Use EMR As The Source Data Collection Tool
 
 

Read about the EMR’s (electronic medical record's) primary purpose: to give providers a flexible tool to document patient encounters and generate appropriate billing for insurance companies.

 
     
Real-World Sleep Assessments Using Wearable Technologies
 
 

Poor sleep patterns are linked to the progression of many diseases. Explore the advantages of assessing sleep from the patient’s home using wearables.

 
     
3 Ways To Unlock The Value Of Real-World Evidence
 
 

Tune in as Castor’s director of solutions consulting, Kristen Harnack, illustrates how a modular approach to clinical technology can help you conduct an RWE study.

 
     
How Clinical Operations Can Accelerate Through De-Risking Clinical Trials
 
 

While clinical trial innovations result in increasingly diverse data sources and study types, discover why this diversity also brings additional concern about patient safety and data quality.

 
     
YPrime eConsent
 
 

At YPrime, we have a passion for empowering the patient through their clinical trial journey and eliminating the barriers and friction that get in their way.

 
     
elluminate Statistical Computing Environment
 
 

Enhance your statistical analyses, automate workflows, and increase programming and analysis efficiencies with the elluminate Statistical Computing Environment (SCE).