Overview

DCTs involve an ecosystem of tools, people, and processes - allowing patients, sites, and sponsors to participate, contribute, and monitor any clinical trial. Successfully executing DCTs often requires multiple disparate solutions integrated across the clinical continuum in order to properly communicate. But what if patients, sites, and sponsors could participate and monitor clinical trials without the integration hassles? Join to hear our experts discuss how to deliver DCTs so everyone wins.

Featured topics

Building decentralized trials for Patients, Powered by Data

Who should attend?

Biotechnology
Clinical Data Management/eClinical
Clinical Laboratory Data
Clinical Research
Clinical Safety and Pharmacovigilance
Clinical Supplies
Clinical Trial Management
CMC/ Good Manufacturing Practice (GMP)
Comparative Effectiveness/Health
Dictionaries/Data Standards
Document Management/eSubmissions
Good Clinical Practice (GCP)
Manufacturing: Drug Substance, Drug Prod
Medical Communication
Medical Writing
Patient Engagement
Pharmacodynamics
Pharmacology
Rare, Orphan Diseases
Regulatory Affairs
Research & Develop/Strategic Issues
Statistical Science
Study Endpoints/Clinical Outcomes

Learning objectives

Participants will be able to understand the common challenges with DCT and RWD and also see probable technological solutions that are in place to address them.

Have an account?

Beyond Decentralized Clinical Trials(DCT) – Building Better Data Ingestion Models for Patients

Overview

Featured topics

Who should attend?

Learning objectives

Be informed and stay engaged.