Is a multifaceted organization that offers a wide range of medical information management services as consultants to the pharmaceutical industry. We provide clinical trial data in drug safety management, clinical data management, medical information reviews, medical writing, and more. Our data management services provide Pharmaceutical and Biotech industries with extensive experience in managing clinical trials across a broad range of therapeutic areas including Medical Devices, Vaccines, and Drugs. Our team of Data managers, Medical Writers, and Drug Safety Physicians are experts in drug safety and pharmacovigilance. Our data management professionals are well versed with a broad therapeutic experience in clinical trials and work diligently to provide cost-effective and seamless services to our clients. With our extensive network of experts and support staff, we are committed to providing our clients with best-in-class service that meets all their needs. 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 expertise. Headquartered in the United States, we have offices in India and are planning to expand our outreach to other regions as well.
