The pharmacovigilance and drug safety data management team covers adverse event data (AE) management with all-inclusive solutions.Increased productivity, improved safety monitoring, and more time for strategic planning are all possible with a model that can easily adapt to changing circumstances. Our knowledge and experience in the fields of pharmacovigilance and drug safety are unparalleled. We work every day to strengthen the clinical trials arena through systems evaluations, processes, SOPs, documentation, technology, and the support of clinical validation and more. Our team members are specialized in: Pharmacovigilance, MedDRA and Drug Safety expertiseIncreased productivity, improved safety monitoring, and more time for strategic planning are all possible with a model that can easily adapt to changing circumstances. Our knowledge and experience in the fields of pharmacovigilance and drug safety are unparalleled. We work every day to strengthen the clinical trials arena through systems evaluations, processes, SOPs, documentation, technology, and the support of clinical validation and more. Our team members are specialized in: Pharmacovigilance, MedDRA and Drug Safety expertise