About Us

At CLINFINITY, we are committed to combining the most flexible, innovative and effective solutions that will enhance the productivity and competitiveness of our clients. Our collective industry knowledge enables us to support our client's goals by improving data quality and accelerating product development. We incorporate a streamlined approach making the best use of each client's time and resources. Our network of experienced Clinical Research Consultants located across the country provide high quality, regional, cost-effective expertise in Study Design, Clinical Trial Monitoring, Medical Writing, EDC, Trial Coordination, Medical Monitoring, Regulatory Management and Project Management. CLINFINITY consultants are experienced in Medical Device studies, Phase I-IV studies, EDC and OTC Switch studies. In addition, we have extensive knowledge of GCP/ICH guidelines including HIPAA and CFR 11. From Monitoring to QA Auditing, we can assemble a team to meet the most demanding requirements.  We offer our clients the benefits of our extensive clinical trial experience in many therapeutic areas. Based on your requirements, we can provide guidance and leadership for the entire trial process, or provide consultative recommendation on specific aspects of your study. Through our experience, we have gained tremendous insight and trust. We know what it takes to get things done - quickly, cost-effectively and with the best results.

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