- medaffairs@deqaseharesearch.ae
- +971 58 665 3631
Welcome to Deqa Wa Seha
Your Global Partner for Comprehensive Clinical Research Services
Deqa Wa Seha is a leading global Site Management Organization (SMO) and Contract Research Organization (CRO) and a trusted partner to global biotechnology and pharmaceutical companies, delivering specialized clinical research services that drive success.
One partner that manages the sites and runs the study — from site activation to data.
27
Years
98%
Study success rate
40–70%
Faster Recruitment
4
Regions
80+
Clients
About Us
Personalized End-to-End CRO for All Clinical Development Phases
Deqa Wa Seha is a full-service Site Management Organization (SMO) and CRO — one partner, one contract, one accountable team that manages the sites and runs the study.
At Deqa Wa Seha, we specialize in delivering tailored clinical research solutions that support the development of groundbreaking therapies. Leveraging deep scientific, regulatory, and operational expertise, we provide flexible and scalable services that address the unique demands of global study execution. Our commitment to patient engagement, data integrity, and regulatory compliance ensures reliable outcomes that help accelerate the path from research to real-world impact.
As a trusted global partner, we collaborate with sponsors to navigate diverse markets and complex protocols while maintaining the highest standards of quality and transparency. Our innovative approach combines cutting-edge technology with a focus on continuous improvement—helping to bring new treatments to patients faster and more efficiently.
Contact us today to discover how our clinical research services can support your next clinical trial.
Global Expertise
Advancing Clinical Research With Precision And Innovation
Full-Service Site Management (SMO)
Full-Service Site Management (SMO)
We run the sites, not just support your study. We manage directly-operated and partner sites end to end: activation, staffing, recruitment, retention, and site-level trial conduct, all under one partner.
Global Recruitment Expertise
Leveraging Local Insights
Tailored recruitment approaches driven by local insights and extensive market knowledge to meet enrollment targets.
Innovative Patient Engagement
Compliance Focus
Implementing patient-focused communications and decentralized methods that improve recruitment success and maximize retention rates globally.
Comprehensive Trial Solutions
Enhancing Recruitment and Retention
Delivering tailored operational strategies that cover all key aspects of clinical research—study design, monitoring, and site management—to optimize trial efficiency.
Patient-Centric Approach
Enhancing Participants Experience
At Deqa Wa Seha, we place patients at the center of every clinical trial. Our strategies focus on enhancing the participant experience.
Global Site Management
Worldwide Access
Access a robust global network of trusted research sites, ensuring fast startup, local expertise, and diverse patient recruitment across regions and indications.
Therapeutic Expertise
Specialized Knowledge
Extensive experience across oncology, cardiovascular, infectious diseases, and other specialties, enabling customized approaches to complex clinical programs.
Clinical Excellence
Driving Innovation Through Collaborative Research
At Deqa Wa Seha, we foster innovation by partnering closely with pharmaceutical and biotech companies. Our comprehensive clinical trial solutions combine scientific expertise, regulatory insight, and advanced technology to accelerate drug development. Through collaboration and patient-focused strategies, we ensure efficient trial execution, rigorous compliance, and high-quality data, delivering impactful results that advance global healthcare.
Patient Recruitment & Retention Solutions
Study Planning & Feasibility
Expertise in Clinical Trial Management
Integrated Site & Vendor Management
Full-Service Site Management (SMO)
Our Process
Our Process: Three Steps to Clinical Trial Success
At Deqa Wa Seha, we provide end-to-end CRO solutions, offering personalized clinical research across all phases for pharmaceutical, biotechnology, medical device, and diagnostic industries. We ensure the seamless delivery of clinical trial services worldwide.
Our process is led by full-service site management — as an SMO, we activate and manage the sites at every stage below, from first patient in to last patient out.
01
Feasibility & Site Activation
Leveraging global site networks and data-driven feasibility assessments, we optimize protocol design, site selection and management.
02
Recruitment & Retention
Equipped with patient-centric recruitment strategies, digital technologies, real-world data, and decentralized trial solutions, we boost enrollment and retention globally.
03
Monitoring & Closeout
Utilizing advanced monitoring techniques, we maintain high data quality. Our comprehensive trial closeout services include data cleaning, monitoring, and reporting.
Our Service
Comprehensive Solutions for Clinical Excellence
Deqa Wa Seha offers comprehensive clinical research services designed to support and accelerate your global clinical development programs. Our solutions are tailored to meet the evolving demands of complex trials and diverse patient populations.
Full-Service Site Management Organization (SMO)
Activates faster, enrolls better, runs smoother. We run and manage the sites, not just the study: our full-service SMO activates directly-managed and partner sites faster, enrolls more patients, and keeps trials running smoothly — all under one partner.
Strategic Partnerships
Our strategic partnerships leverage combined expertise and resources to drive innovation, enhance patient access and address complex trial challenges.
Streamlined Global Procedures
Our harmonized operational framework and standardized processes across regions reduce timelines and minimize regulatory hurdles.
Reliable test results
Our commitment to data integrity and operational excellence ensures that we deliver results that advance therapeutic development and regulatory success.
FAQS
Frequently asked questions
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Participants must meet specific eligibility criteria, which may include age, medical history, and current health conditions. Clinical trials seek both healthy volunteers and patients with specific diseases.
Clinical trials follow strict ethical guidelines and regulatory standards. Institutional Review Boards (IRBs) and regulatory agencies oversee trials to protect participants’ safety and rights.
Compensation varies by study and location. Some trials offer financial compensation for time and travel, while others may provide medical care or treatments at no cost.
Seamless Trial Execution
Our expertise in navigating regional nuances minimizes delays and maximizes operational efficiency globally.
Advanced Data Solutions
Our tailored data strategies enhance decision-making and optimize study performance across global regions.
Patient Engagement Excellence
Our patient-centric models respect local behaviors and preferences, driving enhanced participation in global trials.
Our Results
Global Insight and Regional Expertise
As a full-service SMO, we manage directly-operated and partner sites across four regions — giving us direct control of the levers that drive enrollment speed and quality.
Global trials require tailored recruitment strategies that leverage extensive local knowledge and international experience to deliver timely, compliant clinical trial outcomes across complex global regulatory environments. Our expertise in adapting strategies to regional variations enhances operational efficiency, accelerates patient recruitment, and ensures successful execution of multinational clinical development programs.
Testimonials from
our clients
Elevate your clinical trial success by partnering with us for flawless execution.
SMO · CRO · GlobalCore
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.
