Logo Image
News
Academy
Publications
All PublicationsE-Books
Media
Editorial PodcastsEditorial VideosPeer ExchangePractice AcademyShortsSponsored PodcastsSponsored Videos
More
Conferences
Conference CoverageConference Listing
Columns
All ColumnsA Closing ThoughtClinical Trial InsightsView from BrusselsView from Washington
Resources
AdvertiseBlogsEventsFront & CenterPartner PerspectivesWhite Papers
Webcasts

Subscribe

  • News
  • Academy
  • Publications
  • Media
  • Conferences
  • Columns
  • Resources
  • Webcasts
  • Subscribe
  • Clinical Operations & Strategy
    • Decentralized Clinical Trials
    • Trial Design
    • Investigative Sites
    • CRO/Sponsor
    • Risk-Based Monitoring
    • Protocol Design
    • Clinical Trial Supply Chain
    • Study Start-Up
    • Early Phase Development
  • DEI
    • Industry Initiatives
    • Diversity Action Plans
    • Recruitment
  • Data Management
    • Analytics
    • Electronic Data Capture
    • Real World Evidence
    • Metrics & Benchmarks
  • Patient Participation
    • Integrated Research
    • CRAACO
    • Enrollment
  • Regulatory
    • Institutional Review Board & Ethics Committee
    • FDA
    • EMA
  • Technology
    • Artificial Intelligence/Machine Learning
    • eClinical
    • mHealth
Spotlight -
Conference Coverage|
Peer Exchange|
DE&I|
Editorial Videos|
Clinical Operations & Strategy|
Patient Participation
Advertisement

Joonhyuk Choi

Advertisement

Articles by Joonhyuk Choi

eSource Records in Clinical Research: Keeping it Simple

ByJules T. Mitchel, MBA, PhD,Timothy Cho,Dean A. Gittleman,Joonhyuk Choi,Silvana Cappi,Tom Haag,Jonathan Helfgott,Imogene McCanless,Yong Joong Kim
August 1st 2015

Applied Clinical Trials

How to satisfy regulatory concerns about EDC data integrity and site controls over its source records.

eSource Records in Clinical Research

ByJules T. Mitchel, MBA, PhD,Timothy Cho,Dean A. Gittleman,Joonhyuk Choi,Silvana Cappi,Tom Haag,Jonathan Helfgott,Imogene McCanless,Yong Joong Kim
April 16th 2015

Applied Clinical Trials

Figure 1: The Problem 

i4-845239-1408522739497.gif

Three-Pronged Approach to Optimizing Trial Monitoring

ByJules T. Mitchel, MBA, PhD,Yong Joong Kim,Timothy Cho,Dario Carrara,Sergio Dalla Nora,Michael R. Hamrell,Judith M. Schloss Markowitz,Dean A. Gittleman,Joonhyuk Choi
June 1st 2014

Applied Clinical Trials

Study results using a quality-by-design method, risk-based monitoring, and real-time direct data entry.

Advertisement

Latest Updated Articles

  • i4-845239-1408522739497.gif
    Three-Pronged Approach to Optimizing Trial Monitoring

    June 1st 2014

  • eSource Records in Clinical Research
    eSource Records in Clinical Research

    April 16th 2015

  • eSource Records in Clinical Research: Keeping it Simple
    eSource Records in Clinical Research: Keeping it Simple

    August 1st 2015



Advertisement
Advertisement

Trending on Applied Clinical Trials Online

1

ICON Selects Microsoft as Preferred Technology Partner to Scale Agentic AI Platform Across Clinical Trial Lifecycle

2

ACT Brief: Mixed FSP Strategy, DIA Meeting Trends, and Patient Voice in Oncology

3

ACT Brief: Real-Time Evidence Generation, Protocol Digitization, and Decentralized Trial Flexibility

4

2026 DIA Global Annual Meeting: Where Mixed Models Create the Most Value—and What It Takes to Make Them Work

5

ACT Brief: ICON-Microsoft AI Partnership, DCT Site Burden, and AI-Enabled Neuroimmune Discovery

  • About
  • Advertise
  • Contact Us
  • Editorial Contacts
  • Do Not Sell My Personal Information
  • Privacy Policy
  • Terms and Conditions
Contact Info

259 Prospect Plains Rd, Bldg H
Cranbury, NJ 08512

  • Applied Clinical Trials
  • BioPharm International
  • Cannabis Science and Technology
  • Chromatography Online
  • Nutritional Outlook
  • Pharmaceutical Commerce
  • Pharmaceutical Executive
  • Pharm Tech
  • Spectroscopy Online
  • Turbo Machinery Magazine
IS1
Brand Logo

© 2026 MJH Life Sciences®

All rights reserved.

Home
About Us
News
Contact Us