Your Best For A High Quality Clinical Trial Management
ICRA is a Clinical Research Organization (CRO) that offers clinical and regulatory supports to pharmaceutical companies and any other credible sponsors in Africa and international settings.
ICRA offers feasibility assessment, site selection, clinical monitoring, project management, data management, pharmacovigilance, quality assurance, regulatory affairs, trainings as well as clinical services.
Our CRAs are qualified, appropriately trained and well mentored to go beyond the expectations of the sponsor normally put in an approved Monitoring Plan (MP). For all monitoring activities, CRAs always comply with standards of ICH/GCP and local applicable regulations.
ICRA’s staffs are really committed to the development of your products and take total seriousness, accountability and responsibility to work as an extension of sponsor’s team. Such commitment leads irrevocably to brilliant success of projects.
Our CRAs strive to check where applicable the main aspects of clinical trials particularly the rights, the safety and well-being of human subjects are protected because are the most important considerations and should prevail over interests of science and society.