TrialTrust Global
Clinical Trial Document Writing & Review Services – United Arab Emirates (UAE)
MOHAP / DHA / DOH-Aligned | Ethics Committee–Ready | Globally Trusted
Trusted Clinical Trial Documentation Partner for UAE
TrialTrust, a scientific arm of Zoesoe Exports Pvt. Ltd., provides end-to-end Clinical Trial (CT) Document Writing and Review Services for pharmaceutical, biotechnology, and nutraceutical companies conducting clinical trials in the UAE.
The UAE is a rapidly growing clinical research hub in the Middle East, selected for Phase I–IV, bioequivalence, oncology, CNS, cardiovascular, and vaccine studies, regulated by the UAE Ministry of Health & Prevention (MOHAP), Dubai Health Authority (DHA), Abu Dhabi Department of Health (DOH), and local Ethics Committees. TrialTrust supports sponsors and CROs with scientifically robust, authority-ready documentation, aligned with UAE and international standards.
Since 2008, TrialTrust has delivered 330+ clinical trial documentation projects for clients across Europe, Asia, Middle East, Africa, and LATAM.
Who We Serve in UAE
We work with:
UAE & global pharmaceutical companies
Biotechnology & biosimilar developers
CROs conducting trials in UAE
Generic & branded product manufacturers
Nutraceutical & dietary supplement companies
Sponsors conducting UAE-only or multi-country regional clinical trials
Whether your study is UAE-only or part of a regional MRCT program, we ensure full MOHAP / DHA / DOH and Ethics Committee compliance.
Our Clinical Trial Documentation Services
🧪 Clinical Trial Protocol Writing
Regulatory-ready Clinical Trial Protocols aligned with UAE regulatory standards:
Phase I–IV Clinical Trial Protocols
BA/BE, Pilot & Pivotal study protocols
Pharma, Biotech & Nutraceutical product protocols
Study design, objectives, endpoints & statistical rationale
Inclusion/exclusion criteria & risk–benefit assessment
MOHAP / DHA / DOH & Ethics Committee–aligned formats
📊 Clinical Study Report (CSR) Writing
Comprehensive ICH E3-compliant Clinical Study Reports suitable for UAE and global submissions:
End-to-end CSR writing & medical interpretation
Safety & efficacy evaluation
Tables, Listings & Figures (TLFs)
Investigator & site data integration
Clear regulatory-ready clinical conclusions
📁 Backup & Supporting Documentation
Complete supporting documentation required for UAE authorities and Ethics Committees:
Investigator’s Brochure (IB)
Informed Consent Forms (ICF)
Case Report Form (CRF) review support
Statistical Analysis Plan (SAP)
Literature review & clinical justification documents
🔄 Document Review & Gap Assessment
Independent scientific and regulatory review services:
Gap assessment against:
UAE MOHAP / DHA / DOH requirements
Local Ethics Committees
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
EMA, USFDA & WHO guidelines
Scientific consistency & data integrity checks
🛂 Post-Submission Query Handling
Complete regulatory follow-up support until closure:
MOHAP / DHA / DOH & Ethics Committee query responses
Scientific rebuttals & regulatory clarifications
Deficiency response support
Ongoing authority follow-up until approval
Industries We Support in UAE
Innovative & Generic Pharmaceuticals
Biotechnology & Biosimilars
Oncology, CNS, Cardiovascular & Vaccine Products
Nutraceuticals & Dietary Supplements
Herbal & Botanical Products
Export-driven UAE & Middle East clinical programs
Regulatory Alignment & Compliance
All clinical trial documents are prepared in alignment with:
UAE MOHAP, DHA, DOH
Local Ethics Committees
ICH-GCP (E6)
ICH E3 – Clinical Study Reports
EMA, WHO & USFDA guidelines
Why UAE-Focused Companies Choose TrialTrust
✅ 330+ Clinical Trial Documents Delivered Globally
✅ Strong Experience Supporting UAE & Middle East Clinical Trials
✅ Expertise in Pharma, Biotech & Nutraceutical Products
✅ Authority-Aligned Documentation for MOHAP, DHA, DOH
✅ Reliable Post-Submission & Regulatory Support
✅ Confidential, Accurate & Timeline-Driven Execution
Our Experience Footprint
330+ products supported worldwide
Clients across Europe, Asia, Middle East, Africa & LATAM
Experience in MRCTs, UAE-only, and global lifecycle management
Support for UAE regulatory approvals and global submissions
Our Working Approach
Requirement Understanding & UAE / Middle East / Global Scope Finalization
MOHAP / DHA / DOH & Ethics Committee Strategy Alignment
Clinical Document Writing / Review
Internal Quality & Scientific Review
Client Review & Finalization
Post-Submission Authority Query Handling
Confidentiality & Quality Commitment
All UAE-related projects are handled under strict confidentiality agreements, supported by:
Robust quality control systems
Version control & audit readiness
Scientific accuracy & data integrity assurance
Ensuring regulatory confidence and regional/global acceptance.