Genelife Clinical Research is a contract research organization (CRO) founded in 2010. Genelife is dedicated to provide comprehensive Phase I-IV clinical research services to pharmaceutical, biotech and medical device companies across the globe. We are operating in Europe, USA & Asia. We are a full-service CRO providing study management services that include, but are not limited to: project management, protocol development, clinical site selection and management, clinical and medical monitoring, data management, biostatistics, medical writing, regulatory consulting/support, audits, SEC presentations (Pre-IND presentations) and meetings, Pharmacovigilance studies, Pre-Clinical studies and Scientific Advisory Committee management, and a range of other consulting services. Genelife is a technologically advanced CRO with experienced professionals who apply innovative tools and processes to their clinical development research. Our aim is to provide the best service to our clients through the excellence of our work. This demanding level of professionalism gives belief and security to our clients. We believe that our experience in all aspects of clinical trial management places us in a unique position to assist Sponsor with unparalleled support. Genelife has managed studies ranging in size from single- center/Phase I trials to multi-center/multi-national Phase III trials. Summary:- Genelife offers; performance, reliability, demonstrated therapeutic experience, and responsive customer service that lead to high-quality results. Genelife has the resources and the right approach to deliver the results that will make a project successful.