Our team of qualified clinical research associates, specialists and project managers utilizes innovative databases in our clinical trial services to ensure that all your projects are delivered in a timely manner and meets international standards.
Our team members are certified by the International Conference on Harmonization of Good Clinical Practice (ICH-GCP). They ensure that the integrity of data collected, the rights and safety of the participants, and the quality of the clinical products used to conduct the trials meet international standards. Specifically, our professionals are certified in: GCP for Clinical Investigations of Devices, GCP for Clinical Trials with Investigational Drugs and Biologics (ICH Focus), GCP for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus), and Good Manufacturing Practices.
We recognize the importance of partnerships with academic institutions in driving medical innovation and clinical solutions. Arkans was founded and provides full support of all clinical trial phases, from Ethics Committee submission to patient recruitment.
Our professional team is well-versed in the intricacies of medical device studies and therapeutic areas of clinical research. By drawing from diverse expertise, our clinical research services ensure that your new treatment is fully-researched and reaches successful market access.
Our talented individuals work closely with clinical research centers across Thailand to ensure that we achieve the best possible outcome for each clinical case. Arkans specialists have worked on several multi-center and multi-regional projects – allowing us to navigate through every type of project.
We are recognized for our leading scientific expertise in value proposition strategy development and evidence generation for all stakeholders. Arkans has an established reputation for our strong capabilities in publication and facilitating healthcare decision-making backed by scientific evidence.