CrewFox has vast experience in integrated services in clinical trials for pharmaceutical, biotech, and medical device companies (Phase I–IV). The core competencies include data management, biostatistics, statistical programming, drug safety, pharmacovigilance, medical writing, and regulatory services for pharmaceutical and biotechnology companies worldwide. The team at CrewFox strives to develop the organization on the basis of high standards of professional skills, efficient execution, and a user-friendly work culture for the clients to ensure a smooth project flow, a cost-effective budget, and a successful outcome delivered on time.