Services
Hekma Clinical Research will ensure that the services provided and clinical researches 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.
We are experienced in data management of clinical research studies in the Middle East and Gulf, and in managing national and international studies as a member of society for clinical data management. We use comprehensive clinical data management software with a data management protocol and clear SOP. The executive management team is committed to continuous quality improvement, reviewing quality objectives on a regular basis. Continuous training and testing ensure that clinical research personnel are up to date with all professionally required knowledge.
Hekma is a Clinical research organization. We know the native investigators and the local regulatory process. Having a broad network of researchers in 31 countries, we can manage multi-center studies. We monitor and organize clinical trials and manage clinical sites for national and international pharmaceutical and biotech companies. We share our experience with investigators to facilitate their work. Hekma provides comprehensive product development services for bio- pharmaceutical, medical device, diagnostics and medical data industries.
We welcome cooperation with national and international pharmaceutical companies, Clinical research organizations and investigators in the covered region and beyond.
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.