Clinical Research Organization
Pioneering Clinical Research for a Healthier Tomorrow
Clinical Research Organizations (CROs) design and conduct clinical studies under the sponsorship of the pharmaceutical industry.
Hekma Clinical Research is equipped to design and manage multi-center studies across the Sultanate of Oman and other GCC countries.
Achievements
With nearly two decades of expertise in clinical and pharmaceutical research, our team at Hekma Clinical Research has accomplished the following:
- Managed international epidemiological and clinical studiesacross 40 sites.
- Conducted e-learning courseson GCP and other clinical research training programs (multimedia and text-based).
- Research consultationto epidemiological and clinical research projects with about 4,000 contracts.
- Published 520 medical articlesin international journals.
- Established contracts and MOUswith global pharmaceutical companies and research institutes in France, Germany, the UK, Denmark, Japan, Singapore, the UAE, Tunisia, Pakistan, and others for collaboration in epidemiological and clinical research.
- Launched a dedicated server and softwarefor clinical data management
- Developed a research ethics websitewith comprehensive resources.
- Launched the Hekma Clinical Research websitein English and Arabic.
Hekma-Novarea Partnership
Novarea Inc., a Canada-headquartered company, serves as Hekma’s North American partner, facilitating clinical trial operations, regulatory navigation, site coordination, and market development in Canada and the U.S.
Clinical Data Management
Hekma Clinical Research, manages clinical data in compliance with the Good Clinical Data Management Practices (GCDMP) standards established by the Society for Clinical Data Management (SCDM). Proper clinical data management is critical to the success of clinical studies.
CRA Training in Clinical Research Courses
Our team has developed an online clinical research training package featuring 8 modules:
- ICH-GCP
- Randomized Controlled Trial (RCT) Design & Protocol
- Randomized Controlled Trial (RCT) Registry
- Clinical Research Outcome Reporting (CONSORT)
- Safety Reporting in Clinical Research
- Clinical Research Monitoring
- International Considerations for Clinical Studies
- Clinical Research Ethics
Research Ethics
At Hekma Clinical Research, ethical adherence is the cornerstone of all research projects and clinical trials. We follow our “Code of Ethics in Clinical Research”, which reflects our commitment to human dignity and compliance with local and international ethical standards.
We also offer an online training package on ethics in medical research.
Online Training Course: Ethics in Scientific Research
Hekma has designed and delivered a specialized ethics in research training course, developed by professors and experts in medical ethics. The program includes five courses:
- Fundamentals and History of Research Ethics
- Research Ethics Committee
- Informed Consent
- Ethics in Clinical Research
- Ethics in Publishing Results
These courses cater to researchers, doctors, healthcare staff, ethics committee members, research center personnel, and students across disciplines. We highly recommend them for all researchers.
Alternatively, you may contact us at:
cro@HekmaSolutions.net