top of page
shutterstock_373568524.jpg

Cloud-based clinical research support system
DokodemoForm® EDC

Easy setup and can be started in as little as one month

Start from as little as one month

Easy drag and drop setup

Go Live as you wish

Cloud-based clinical research support system

Easy-to-use plan for

Father and Son Playing
White Structure

Why EDC ?

01

Improved data entry efficiency and accuracy

The EDC system allows multiple people at multiple facilities to enter data simultaneously, and performs automatic error checking to eliminate inaccurate data and mistakes.

The audit trail makes it clear who modified what and when.

This greatly reduces the verification work.

02

Efficient data management

In the EDC system, all data is managed centrally, and data from multiple facilities and research institutes can be easily integrated and output in CSV format.

Aggregation and analysis is possible in real time, facilitating quick decision-making.

03

Increased data safety and security

Data is stored securely in the cloud or on servers, reducing the risk of loss or damage.

EDC systems are compliant with regulations such as FDA and GCP, and can meet the audit requirements for clinical trials.

ジョン_edited.jpg

Subscription Plan for Small Clinical Trials
Dokodemo- Form® IIS
release

Easy setup, new DIY EDC plan now available!

Monthly fee only. Go Live schedule can be set as you like.

Would you like to experience a new era in clinical research?

DokodemoForm® IIS

A subscription plan is now available that allows you to use DokodemoForm®EDC at a great price for small investigator-initiated studies.

By configuring and building your own system, you can meet delivery deadlines as you wish

No initial costs, which can be expensive, so you only pay for what you use

Optimized for short study periods and small target case numbers

Want to give DokodemoForm® IIS a try?

 

医師

No initial cost

Subscriptions do not require expensive initial costs, so you can start anytime, anywhere.

在宅勤務

Easy to set up for anyone

Easy drag-and-drop setup allows you to set it up without any specialist knowledge.

chrome_aIzzBm2Ie3.png

Peace of mind with security

ES/ER guidelines, GCP, GPSP and 21CFR part 11 ISO/IEC 27001:2005 Audit compliant

新しいステッカー

v.2.1 available

Available in the latest version v.2.1

DokodemoForm® EDC v.2.1 Released

chrome_l8htJxyC6D.png

All Questionnaire PDF

  • Grey LinkedIn Icon

It is now possible to output all questionnaires in PDF format at once from the data management screen.

Use a spreadsheet

Bulk download of queries

  • Grey LinkedIn Icon

It is now possible to download "queries" in bulk from the data management screen.

Medical Consultation

Output of a list of examinee status by facility

  • Grey LinkedIn Icon

It is now possible to print out a list of subject status for each facility from the attending physician screen.

Breaking down the numbers

Change of subject registration number

  • Grey LinkedIn Icon

It is now possible to change the registration number from the responsible physician's screen.

Recycled Box

Deleting/Restoring Subject Data

  • Grey LinkedIn Icon

It is now possible to delete subject data from the doctor in charge's screen.

document

Features List

  • Grey LinkedIn Icon

The list of features of Dokodemo Form EDC is as follows:

Here

Easy-to-understand input screen

Missing data and status are clearly visible at a glance, making the next task immediately obvious.

chrome_S6y2gD6bnr.png

easy
Form Settings

Easy drag and drop setup.

Anyone can use it without training or manuals

It's intuitive to use.

Progress on site
real time

A graph that visualizes on-site progress in real time, allowing you to grasp the project status at a glance and make quick decisions.

Standard process of setup

Steps to start using "Dokodemo Form®EDC"

For more information,
Please join our

Members!

For more information, please register at the "Members only" bar at the top of the homepage.

Pharmacovigilance
service


・System Implementation and Project Management
・Risk-based Computer System Validation
21 CFR Part 11, Gamp 5
・Periodic Regulatory Reporting
PMDA
・Custom Reporting
・Data Analysis and Cleansing
・Training
・Data Migration

登録する
手を握る.jpg

For EDC demos and inquiries, please click here

送信ありがとうございます

bottom of page