Services
Hekma Clinical Research will ensure that the services provided and clinical researche are performed to the highest standards, in compliance with FDA regulations and ICH-GCP guidelines and especially according to the rules of regulatory authorities in local countries.
Clinical Research
From Phase I to IV trials, we deliver end-to-end clinical research solutions. Our expert teams ensure compliance, efficiency, and patient safety, helping you bring innovative therapies to market faster. Partner with us for seamless study execution.
Data Management
Accurate, secure, and real-time data drives successful trials. Our advanced data management services ensure high-quality collection, cleaning, and analysis—reducing risks and accelerating your path to regulatory approval
Biostatistics
Power your research with robust statistical insights. Our biostatistics team designs trials, analyzes complex data, and delivers actionable results—ensuring your study meets regulatory standards and achieves scientific excellence.
Medical Writing
Clear, compliant, and compelling documentation is key to trial success. We provide high-quality protocols, reports, and regulatory submissions—turning complex data into concise, submission-ready documents.
Innovation
Embracing cutting-edge technologies to redefine clinical research. From AI-driven analytics to digital trial solutions, we integrate innovation at every stage to enhance efficiency, accuracy, and patient engagement.
Smart Applications
Streamline trials with our custom digital tools. From ePRO to EDC systems, our smart applications improve data accuracy, site productivity, and patient participation—making research faster and more reliable.
Research Bioethics
Ethics at the core of every study. We ensure compliance with global ethical standards, safeguarding participant rights and data integrity while maintaining transparency with regulators and stakeholders.
Regulatory Affairs
Regulatory Affairs & Compliance ensures clinical trials meet global standards (FDA, EMA, ICH-GCP). We handle submissions, audits, and approvals to accelerate timelines while maintaining ethical and legal integrity.
Turn insights into action and revenue into results
Hekma Clinical Research is a Clinical Research Organization (CRO) based in Muscat, Oman. Our full-service CRO is now an important partner for universities, research centers, scientific societies as well as pharmaceutical and medical device industry in the Middle East and North Africa (MENA), and Gulf region.
Research Network
Knowledge Synergy, Innovation Acceleration
Middle East / GCC
Hekma Clinical research is a regional Clinical research organization. We know the native investigators and the local regulatory process in different countries. Having a broad network of researchers in countries located in MENA and Gulf region, we can manage multicenter studies in parallel with the multinational companies across the world. This network makes it possible and facilitates conducting international research projects professionally.
International Partners
