What You Will Learn

Recent improvements in clinical trial technology hardware, software, and applications have led to them being more user-friendly. These improvements have changed the implementation of clinical trials, allowing remote participation because of the increased accessibility and use of technology. Through electronic consent, electronic diaries, electronic clinical outcome assessments, wearables (e.g., a GPS or heart rate monitor), and telehealth, Decentralized Clinical Trials (DCTs) allow better access to clinical trials than ever before. In this webinar, MMS data managers will review the basics of decentralized clinical trials and expand on how to address challenges that may arise when working on a DCT.

Attendees will learn about:

  • What constitutes a decentralized clinical trial?
  • An overview of different DCT models, full vs. hybrid, and how to differentiate between them
  • Optional modules and add on applications
  • How to manage challenges that may arise, including impacts to potential timelines

Who Will Benefit from Attending?

  • Data Managers
  • Project/Program Managers
  • Database builders
  • Clinical operations team members
Our Experts
Doreen van Huyssteen
Associate Director, Clinical Data Management
Ronelle Adlem
Senior Manager, Clinical Data Management
Krista Bossi
Associate Manager, Clinical Data Management

Register Now

Suggested For You

webinar

September 26th, 2024

Regulatory Pathways for Nonprescription Drugs: A Deep Dive into OTC Monograph Reform and FDA Guidance

webinar

January 18th, 2024

Best Practices for Data Visualization in Pharma, presented by MMS Holdings Data Science leaders

webinar

January 18th, 2024

How to Use Machine Learning in Clinical Research Right Now

webinar

January 18th, 2024

Tips for Efficient and Effective New Drug Application (NDA) Submissions

webinar

January 17th, 2024

Strategies for Navigating ICH E9(R1): Considerations for Using Estimands and Sensitivity Analysis in Clinical Trials

webinar

January 17th, 2024

How to Submit Non-Clinical Data to CBER Using SEND : Understanding New FDA Requirements

webinar

January 17th, 2024

Using Natural Language Processing to Curate Unstructured Electronic Health Records into Research Ready Datasets

perspectives

July 23rd, 2024

PSI 2024 Ignited Conversations on External Data Sources, Requirements for Estimands, and Bayesian Methodology for Statisticians in Pharma

perspectives

December 27th, 2023

Clinical Data Science: Five Ways it Evolved from Clinical Data Management

perspectives

October 17th, 2023

Proven Ways to Meet Key Study Start-up Timelines within Clinical Data Management

perspectives

September 25th, 2023

Clinical Data Managers Should Do These Three Things for Any Post-Production Changes

perspectives

March 16th, 2023

10 Things to Consider When Discussing and Planning a Decentralized Clinical Trial (DCT)