Target Health

Clinical Trial Software Developed by CRO

Software Development since 1999

Clinical trial software system is compliant with FDA 21 CFR Part 11, Electronic Records with Audit trail; Electronic Signatures. The goal of Part 11 is to protect the electronic data within software systems.

Conducted more than 1000 studies globally

Clinical trial software system is being used globally in North/South America (US, Canada, Brazil, etc.), Asia (China, Japan, Korea, etc.), Europe (UK, German, France, Denmark, Switzerland, etc.)

Drug/Device Approvals globally

Using Target Clinical Trial Software Suite, Drugs and Devices have been approved from US, Canada, EU, Japan, etc.

Versatile and Reliable Software Solution For Clinical Studies of All Sizes

eSource Software

Target Health eSource software enables the Paperless Clinical Trial

Patented and Proven

Our patented eSource is proven by our CRO and in use every day

Globally Used

By Sponsors and at sites around the world

Target Health e*Studio

Working for Sponsors and CROs of all sizes and types

Target ePRO/Mobile

Target e*CTR
Patented eSource Solution

Target eConsent

Target e*CRF® + Target e*Studio
(Target e*ICF™/Target e*Pharmacovigilance)

Target Software Suite

Fully Integrated Paperless Clinical Trial Solution

Target Document

Target e*Safety

Target IWRS (Randomization + IMP)

Target Encoder

Built for Complete Study Application Cycle

Build, Test, Deploy

Go-Live Cutover

Easy Installation
Build Form (Copy & Paste from Master study)
Edit Check Configuration
IC Form Configuration

eInformed Consent

Subject Registration

Patient No. Registration
eInformed Consent
Patient Signature
Investigator Signature

Screening

Medical Screening

Demographics
Physical Examination
Medical History
Adverse Event

Treatment

Data Entry

Enrollment
Treatment
Safety Data
Efficacy Data

Reporting & Exporting

Standard Built-in Reports

Customized Report for a study specific

Data Listings and Tables

Data Exports in Pre-Defined SAS dataset