๐Ÿ‡ฆ๐Ÿ‡ช Clinical Data Capture in United Arab Emirates

EDC Software for Clinical Trials in the UAE

MOHAP, DHA and DOH-aligned EDC for the UAEโ€™s growing clinical research sector

From Dubai and Abu Dhabi to the northern emirates, capture compliant eCRF data with Elysium Clinical Trials EDC โ€” the platform that matches the pace of the UAEโ€™s medical research expansion.

๐Ÿ‡ฆ๐Ÿ‡ช
United Arab Emirates
EDC for clinical research teams
  • Compliant audit trails & e-signatures
  • Local-currency pricing: AED 4 to USD
  • 14-day free trial, no credit card
  • Deploy in days, not months

The UAE has become one of the fastest-growing clinical research destinations in the Middle East. Emirate-level authorities โ€” the Ministry of Health and Prevention (MOHAP), the Dubai Health Authority (DHA) and the Department of Health in Abu Dhabi (DOH) โ€” have modernised clinical trial frameworks, shortened approval timelines and created incentives for international sponsors to run regional studies in the country.

With that momentum comes a stricter-than-ever inspection culture. Sponsors and CROs operating in the UAE need eCRF systems that satisfy the data-integrity expectations of federal and emirate authorities while supporting bilingual sites and internationally standardised trials. Elysium Clinical Trials EDC was designed for exactly that balance.

This page explains how Elysium supports your UAE trial submissions, which authorities matter, and what the platform costs in UAE dirhams.

Compliance

Local Regulatory Authorities & Data Integrity

Elysium is engineered for the record-keeping expectations of the authorities that govern clinical research in United Arab Emirates.

MOHAP

The Ministry of Health and Prevention oversees clinical trials in the federal and northern emirates. Elysiumโ€™s audit-trail and electronic-signature capabilities support the data requirements that accompany MOHAP trial approval.

Dubai Health Authority (DHA)

The DHA regulates research conducted at Dubai-based healthcare facilities, including approval and ongoing oversight of clinical research. Aligned data management makes DHA monitoring visits and audits faster to satisfy.

Department of Health โ€“ Abu Dhabi (DOH)

DOH governs clinical research in Abu Dhabi, including healthcare facility licensing and research permits. Elysium helps you keep a clean, attributable record trail for DOH requirements.

National Committee of Bioethics (NCBE)

Ethics review for health research across the Emirates, with national and institutional committees reviewing protocols. Clean system records underpin the documentation ethics committees request.

UAE trials are typically approved at the emirate level first, and international sponsors commonly use one UAE site to anchor Gulf-region enrolment. Because Elysium lets you manage multiple sites and languages under one study, it fits both a single-centre UAE trial and a wider Gulf or MENA roll-out from the same environment.

Platform

A Complete Electronic Data Capture Platform

Everything your study team needs, from first CRF draft to database lock and export.

Drag-free eCRF Builder

Design case report forms with validation, skip logic and required-field rules โ€” no code.

Study & Subject Management

Manage sites, visits, subjects and ePRO/pROM instruments from one workspace.

Security & Access Control

Role-based permissions, two-factor-ready logins, encryption in transit and at rest.

Queries & SDV

Raise, answer and close queries; schedule source-data-verification tasks for monitors.

Audit Trail

Every edit, signature and query is attributed, time-stamped and non-destructive.

Export & Reporting

Export to CSV, Excel, JSON or CDISC ODM; API access for downstream pipelines.

Electronic Signatures

e-sign at form, visit or study level with full linkage to the signer and timestamp.

Randomization

Coding and allocation management with support for commonly used randomization schemes.

Medical Coding

MedDRA/WHO-Drug-style term coding within the same environment you enter data.

Onboarding

From Sign-Up to First Data in Three Steps

1
Create an Account

Sign up for a 14-day free trial. No credit card, no procurement delay โ€” your team can explore immediately.

2
Build Your CRFs

Model your study, sites and visits, then assemble eCRFs with the visual builder โ€” most studies are live within a day.

3
Enroll & Monitor

Invite site staff, enroll subjects, run queries and SDV, then lock and export when your database is clean.

Why Elysium in United Arab Emirates

Built for how research teams in United Arab Emirates actually work

  • One study environment supporting Arabic and English data entry side by side
  • Audit trails and electronic signatures that meet federal and emirate data-integrity expectations
  • Remote monitoring workflows for international sponsors overseeing UAE sites
  • Multi-site structure ready for Gulf-region expansion as your next site comes online
  • Quick eCRF build with no coding, so study teams at any UAE facility can self-serve
  • Data exports for your regional or global data management pipeline

UAE research teams are aggressive adopters of technology, and their sites expect modern tools. Elysium gives CROs and sponsors a scalable, cost-managed eCRF platform โ€” with dirham-visible pricing and support that understands both the regulatory path and the practical realities of running studies across emirate boundaries.

Pricing

Pricing for United Arab Emirates in UAE Dirham

Transparent, local-currency figures so you can budget without doing the forex math. Billing on your invoice is in US dollars; equivalents are shown at the current rate.

SALE
Starter

For small studies and independent researchers

AED 110 /mo
AED 184/mo
Save 17% โ€” AED 91/mo billed yearly
AED 153/mo billed yearly
  • 5 Studyies
  • 50 Subjects
  • 5 Users
  • 2GB Storage
  • Core EDC
  • CSV Export and Import
  • Audit Trail & Reports
  • Internal Messaging System
  • Query Management
Get Started
Most Popular
SALE
Professional

For growing research teams and CROs

AED 183 /mo
AED 363/mo
Save 17% โ€” AED 153/mo billed yearly
AED 303/mo billed yearly
  • 15 Studyies
  • 500 Subjects
  • 15 Users
  • 5GB Storage
  • REST API Access
  • Core EDC
  • CSV / Excel Export
  • Audit Trail and Reports
  • Internal Messaging System
  • Query Management
Get Started
SALE
Enterprise

For organizations running multiple concurrent studies

AED 1,097 /mo
AED 1,831/mo
Save 17% โ€” AED 917/mo billed yearly
AED 1,529/mo billed yearly
  • 100 Studyies
  • 5,000 Subjects
  • 100 Users
  • 25GB Storage
  • REST API Access
  • Core EDC
  • All Exports / Import Options
  • Audit Trail and Reports
  • Query Management
  • Priority Support
  • Internal Messaging System
  • Medical Coding (ATC/DDD, WHO ICD-10, LOINC)
  • REST Api Access
  • Desktop app (works offline as well)
Get Started
SALE
Unlimited Plan

For large CROs and enterprise sponsors

AED 1,831 /mo
AED 5,501/mo
Save 17% โ€” AED 1,529/mo billed yearly
AED 4,587/mo billed yearly
  • Unlimited Studyies
  • Unlimited Subjects
  • Unlimited Users
  • 100GB Storage
  • REST API Access
  • All Advanced Features
  • Dedicated Support
  • Custom SLA
  • Complete System Training
  • Internal Messaging System
  • Medical Coding (ATC/DDD, WHO ICD-10, LOINC)
  • *Sensitive Medical Coding (medDRA and WHODrugs)
  • REST API Access
  • Desktop app (works offline as well)
Get Started

Need a dedicated EDC built for your organization?

Custom study types, self-hosted or private-cloud deployment, local regulatory and language support, dedicated SLAs, SSO, and audit packs for United Arab Emirates-based sponsors and CROs.

Or start with a free 14-day trial โ€” no credit card needed.
FAQ

Questions about EDC for United Arab Emirates

Which UAE authorities does Elysium align with?

Elysium supports the data-integrity and record-keeping expectations of the three main research regulators in the UAE: MOHAP, DHA and DOH, plus the ethics-review framework led by the National Committee of Bioethics. Approval itself always comes from each authority for your specific trial.

Does Elysium support Arabic and English?

Yes. Form labels, instructions and eCRF content can be authored in Arabic, English, or both within the same study, which suits UAE sites where participants and staff may be bilingual.

Can an international sponsor monitor a UAE trial remotely?

Yes. Monitors and CRAs are given role-limited access and can review data, raise queries and perform source-data-verification checks without travelling, while the audit trail records every action.

Is billing available in UAE dirhams?

Prices shown on this page are dirham equivalents for your budgeting. Your subscription is billed in US dollars, and an invoice is issued for each charge; see the pricing section for current AED-equivalent figures.

How fast can a UAE site go live?

Once an account is active (same day for most teams), a typical oncology or registry-style eCRF can be built in a day and a pilot study in under a week. There is no installation or IT dependency at the site.

Ready to start your United Arab Emirates clinical study?

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