- medaffairs@deqaseharesearch.ae
- +971 58 665 3631
CRO Services — Full-Service Clinical Trial Management
End-to-end clinical development, run by one accountable team — from first patient in to last patient out.
As a full-service Contract Research Organization, Deqa Wa Seha manages every stage of your trial under one roof: study start-up, clinical operations, monitoring, data, safety, and reporting. Paired with our dedicated Site Management (SMO) capability, we can run the study and the sites together — so your program activates faster, enrolls better, and runs smoother across global markets.
One contract, one team, and one line of sight from protocol to final report.
Sponsors lose time and control when a trial is split across disconnected vendors. Deqa Wa Seha integrates the complete clinical development lifecycle into a single, accountable model — with the option to combine our CRO services with our in-house Site Management Organization (SMO) for true end-to-end delivery.
Sponsors and CROs work with us in the way that fits their program.
As your full-service CRO — or as the regional partner who runs the sites while you keep program oversight.
Your Full-Service CRO
When you need a single accountable partner, we manage the entire trial end-to-end — study start-up, clinical operations, monitoring, data, safety, and reporting — under one contract and one team.
Your Regional Site-Execution Partner
Already have a CRO — or are one? Many international sponsors and CROs engage us as their regional site-execution partner: we run the sites on the ground across our regions while they retain program oversight. It is the fastest way to reach our patient populations and regional expertise without changing your lead CRO.
Delivered through our Site Management (SMO) capability — see our Site Management (SMO) page.
Numbers that show up in every study we run.
27 Years
of clinical research expertise
98%
Study success rate
Phase I–IV
Full lifecycle coverage
4 Regions
Middle East · APAC · North America · Africa
200+ Studies
80+ clients · 60+ sponsors
40–70%
Faster recruitment timelines
A complete set of CRO service lines that cover the full drug, biologic, and device development lifecycle.
Delivered as a full package or selected to fill capability gaps in your own program.
Clinical Operations & Project Management
A dedicated study team owns day-to-day execution — logistics, timelines, budgets, and coordination — serving as your single point of contact and accountability from kickoff to close-out.
Study Start-Up & Site Activation
Feasibility, site identification and selection, essential-document collection, contracts and budgets, and rapid activation — getting qualified sites open and enrolling without delay.
Clinical Monitoring (On-Site & Risk-Based)
Experienced clinical research associates deliver on-site, remote, and risk-based monitoring, with source data verification and issue resolution that protect data quality and participant safety.
Regulatory & Submissions Support
Regulatory strategy and submission management for global markets, including document preparation, lifecycle maintenance, and coordinated approvals — delivered with local market knowledge across our regions.
Data Management
Electronic Data Capture (EDC) build and validation, database design, data cleaning, query management, and lock — producing clean, defensible datasets ready for analysis.
Biostatistics & Statistical Programming
Statistical analysis plans, randomization, interim and final analyses, and Clinical Data Interchange Standards Consortium (CDISC)-aligned programming that stand up to scrutiny.
Medical Writing & Scientific Publications
Protocols, investigator brochures, clinical study reports, and manuscripts — clear, compliant, and publication-ready scientific documentation.
Pharmacovigilance & Drug Safety
Safety monitoring, case processing, expedited and periodic reporting, and signal management to keep participants protected and your program compliant.
Medical Affairs & Medical Monitoring
Independent medical oversight, protocol and eligibility guidance, and medical monitoring across the study lifecycle.
Quality Assurance & Inspection Readiness
Documented quality systems, audits, SOP governance, and continuous inspection readiness — built in by default, not bolted on.
Real-World Evidence & HEOR
Observational studies, registries, and health-economics and outcomes research that extend value beyond the interventional trial. See our HEOR page for the full offering.
Site Management (SMO) Integration
Combine any CRO engagement with our dedicated Site Management Organization to run and manage the sites directly — one partner for the study and the sites. See our Site Management (SMO) page.
We design, manage, and deliver trials across the full development spectrum.
Delivered as a full package or selected to fill capability gaps in your own program.
Phase I
First-in-human and early safety, tolerability, and pharmacokinetics — with the operational rigor and speed early decisions demand.
Phase II
Proof-of-concept and dose-finding studies that generate the efficacy and safety signals to guide go/no-go decisions.
Phase III
Large, multi-site confirmatory trials — coordinated across our regional network for consistent, high-quality delivery at scale.
Phase IV
Post-approval, real-world, and observational studies that confirm long-term safety and demonstrate value in practice.
A full-service CRO with a genuine regional advantage — and the site-level control few competitors can offer.
CRO + SMO Under One Roof
The rare partner that both manages the study and runs the sites — one contract, one team, one accountable outcome.
Regional Depth, Global Standards
Deep local knowledge across the Middle East, APAC, North America, and Africa, delivered to world-class operating standards.
Access Others Cannot Reach
A population of 200+ nationalities, large treatment-naïve pools, and a high prevalence of rare and inherited conditions.
Culture- & Faith-Sensitive Delivery
Arabic-first workflows and culturally attuned engagement that lift enrollment and retention where generic approaches stall.
Trained-Staff Pipeline
GlobalCore Academy continuously feeds qualified, certified staff into our own teams and sites — a capability few regional CROs can match.
Proven Track Record
27 years of expertise, a 98% study success rate, and 200+ studies delivered for 80+ clients and 60+ sponsors.
Full-service CRO, dedicated SMO, or both — working as one.
Whether you need a full-service CRO, a dedicated SMO, or both working as one, Deqa Wa Seha delivers clinical trial management to a world-class standard — close to your patients, across global markets.
- medaffairs@deqaseharesearch.ae
- +971 58 665 3631
- Unit 823 Al Irshad Street, Al Hisn, Abu Dhabi, UAE
Three Ways We Partner With You
Deqa Wa Seha brings site management, clinical research, and workforce training together under one organization — so sponsors can run the sites, run the study, and build the team through a single partner.
