eSource

Your Trial's Data Capture, Simplified.

Never miss a data point or procedure through turn-by-turn guidance for all your visits.

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Benefits

Built for Both Sides of the Ecosystem

Turn-by-turn guidance

Never miss a data point or procedure. The platform walks your team through every visit step by step.

Digitalized workflows

Eliminate paper-to-digital re-entry and reduce input errors with logic-based data fields.

Realtime visibility

Monitor your trial with cloud-based one-stop data access, enhancing protocol compliance and early deviation detection.

How it Works

onwardaccess.com/protocol/soa
Schedule of Activities
Summary of procedures by visit
Procedure
Screening
Day −28 to −1
Baseline
Day 1
Week 2
Day 15 ±2
Week 4
Day 29 ±3
Informed Consent
Eligibility Assessment
Vital Signs
Laboratory Tests
Concomitant Medications
RequiredNot required

Key Highlights

USDM-Ready. Convert structured USDM protocols into ready-to-deploy study forms in days.

Drop your .usdm file hereorChoose File
eSource Configuration Ready

No-Code Customization. Build the fields flexibly and rapidly to fit your protocol's needs without code.

Add Field
Text
Number
Dropdown
Date
Demographics
Participant ID
Text
Sex
Select
Height (cm)
Number
Date of Birth
Drop field here

Multilingual. Operate in your language of choice with instant system-wide translation.

English (Default)
Thai
Bahasa Indonesia
Tagalog
Vietnamese
Edit Languages

21 CFR Part 11 Compliant. Equipped with access controls, audit trails, and e-signature.

Audit Log
15:41
13 May
Baseline Visit: Blood Pressure updated to 120 mmHg
M. Lim
15:39
13 May
Demographic: Age updated to 50
A. Muller
15:38
13 May
User P23 added to Study
S. Aminah

Cloud-based. Fully accessible from your mobile and PC regardless of geographical location.

ONWARDAccess accessible across laptop, tablet, and phone

Get In Touch

ONWARDAccess eSource & ePRO captures your clinical trial data on one centralised platform.

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