InClinica specializes in leading companies through all stages of the clinical trial process. Our experience in drug and device development and access to world-class experts, who are critical to trial design and execution, lead to a better anticipation of common and not-so-common mistakes, oversights and assumptions that can derail a study.
InClinica serves all phases of clinical development, with particular strength assisting small to mid-sized companies who are entering first-in-human and phase 2 studies or who need to generate data related to 510k clearance, a de novo 510k application, or a PMA.
An experienced clinical CRO can be the difference between the success or failure of a clinical trial. Discover how InClinica can help move your molecule or your device successfully toward regulatory approval.
Life-Changing Clinical Trials
Get to know InClinica’s leadership team as they share their experiences and personal stories involving life-changing clinical trials. The unique expertise, passion, and team-oriented culture of InClinica ensures a positive relationship with their clients, all while advancing patient care.
Meet the Team!
Meet our senior leadership team, who bring a wealth of experience in drug and device development and clinical trial management. With deep experience in multiple disease categories, access to world-class experts and a track record of timely, successful completion of trials, we invest ourselves fully in your success.