Newsletter | January 10, 2023

01.10.23 -- How One Big Pharma Company Is Embracing Digital Technologies

 
     
 
     
 
 
 

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
     
How One Pharma Company Is Embracing Digital Technologies
 
 

The increased demand for hybrid and decentralized approaches to clinical trials has increased the use of digital devices and other tools that will make studies more patient-centric. Sanofi is one of the companies leading the way in getting devices into the hands of patients.

 
 
 
 
     
Sponsors And CROs Race To Implement A Connected CTMS-eTMF
 
 

A must for all clinical leaders, this webinar shares strategic, operational, regulatory, and financial benefits of a seamless CTMS and eTMF integration. Watch the webinar to find out why CTMS-eTMF integration has increasingly become imperative for sponsors and CROs around the world.

 
     
eSource Makes The eCRF Reliable, Accurate, And Timely
 
 

eSource is the bridge between the protocol and the eCRF fields. To understand why, discover the need to understand what each does.

 
     
How EDCs Are Changing The Game In Clinical Research
 
 

Explore all things EDC in this article: what it is, how researchers can use it in clinical trials, its numerous benefits, and examples of how these translate into the real world.

 
     
The False Economy Of Paper Diaries In Clinical Trials
 
 

Paper diaries may appear cheaper, but there are hidden costs that make a digital eCOA solution much more affordable in your clinical trial.

 
     
How Cenduit IRT Rescued A Multicountry, Multisite Oncology Study
 
 

After go-live, the sponsor learned its study did not fit the existing IRT solution, affecting data quality, timelines, and drug supply shipments. The legacy system’s medication management algorithm could not support the required flexibility in the supply chain. The trial included an adaptive cohort design. Read how Cenduit delivered a high-quality study achieved through innovation, close client collaboration, and expert project management.

 
     
The Anatomy Of An Electronic Case Report Form (eCRF)
 
 

In this blog, walk through some of the terms that need to be known before embarking on the design of an electronic case report form (eCRF).

 
     
Medidata Decentralized Clinical Trials Program
 
 

Watch this brief video to see how the industry’s only scalable, end-to-end offering for decentralized clinical trials can connect trial experiences for patients, sites, and sponsors.

 
     
Medrio EDC: Simplicity Without Compromise
 
 
Clinical trials are complex and time-consuming, but using your EDC shouldn’t be. Medrio EDC was purpose-built for sponsors, sites, CROs, and clinical researchers to eliminate inefficiencies. Our intuitive electronic data capture (EDC) solution was designed to keep you in full control of your study data by offering cutting-edge flexibility without unnecessary complexity.
 
     
Orchestrated Study Start-Up
 
 

Learn how the IQVIA Investigator Site Portal reduces activation timelines and eliminates site frustrations by automating processes and providing complete oversight to study teams.