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Please Wait... Skip to main content What We Do Bioclinica Cloud Medical Imaging Oncology Neuroscience Musculoskeletal Cardiovascular NAFLD / NASH Additional Therapeutic Areas Regulatory Leadership Clinical Adjudication Pharmacovigilance Drug Safety Services Drug Safety Technology LitTrace PVTrace SigTrace Regulatory Affairs IT Services Randomization & Trial Supply MGMT Interactive Response Technology (IRT) Trial Supply Optimization Site & Patient Payments Site Payments Business Process Outsourcing (BPO) Service Budgets Patient Payments Payment Portal Electronic Data Capture Cardiac Safety ECG Measurements Thorough QT Studies Blood Pressure Remote Telemonitoring Pulse Wave Analysis Protocol Design and Expert Reporting WebHeart Platform WebHeart Client Portal Expertise Scientific Expertise Regulatory Expertise Key Acquisitions Clinical Trial Management System Resources Blog White Papers & eBooks Webinars Case Studies Thought Leadership Scientific Publications Books and Book Sections Authored Publications Bioclinica Studies Abstracts and Posters Clinical Trial Articles News & Events Press Releases Events Media Contacts About Management Careers Current Opportunities Life at Bioclinica Compensation & Benefits Offices Contact Search form Search PORTAL youtube Offering Deep Insight into Key Areas of Clinical Development COVID-19 Update: How Bioclinica is Continuing to Support Our Customers and Employees READ MORE Visit Bioclinica at DIA 2017 in Booth #1027 -- Clinical trials are complex, and traditional solutions are either monolithic or fragmented. But the most successful trials require the ability to see key details and uncover hidden insights. Bioclinica creates clarity in your clinical trials—so you can make better decisions. Where can you benefit from more clarity? Show All Patient Engagement Trial Technology Patient Safety Study Start Up Scientific & Medical Expertise A purpose-built, end-to-end, randomization and trial supply optimization platform. A full service solution providing high quality & timely clinical databases. Greater efficiencies in study management process through technology integrations. See more deeply into essential imaging data and uncover evidence others might miss. Meeting the needs of the evolving regulatory and clinical trial cardiac safety arena. Fast, accurate insight from forecast to final payment. Specialized drug safety across all therapeutic areas. Determine the efficacy and safety endpoints needed to analyze clinical trial outcomes. Quickly and easily create and compare supply scenarios against trial objectives. Flexible, scalable and agile by design. See More Clearly Bioclinica helps companies develop new life-improving therapies more efficiently and safely. Successful clinical trials require the ability to see key details and uncover hidden insights, and Bioclinica’s scientific, medical, and domain experts bring a unique mix of insights across the product lifecycle to reduce “pain-points” and enhance development efficiency and effectiveness. Upcoming Events Biomed 2020 - Tel Aviv, Israel - September 7, 2020 View All Events Leader in Clinical Trial Management Solutions Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely. Quick Links: Contact Us Careers Help Search Site Map Terms of Use Privacy Policy UK Modern Slavery Act Statement Language: Ready for a centralized view into your studies but don’t want to take on the risk of procuring a CTMS? With our rap… https://t.co/uognAzsgG3 Bioclinica (2 days ago) Minimize the risk of not having enough medication at a site to assign to a subject with our end-to-end #RTSM soluti… https://t.co/SawP0PaioB Bioclinica (3 days ago) An #EDC can be both cost-effective and flexible enough to manage studies of all sizes and complexities. With an int… https://t.co/lE46N3febr Bioclinica (2 weeks ago) Trennic Data Services chooses Bioclinica #EDC Solo to build & manage studies on their own. “It is the easiest and m… https://t.co/FJK73cmMbN Bioclinica (2 weeks ago) Learn why pharma, biotech, and medical device sponsors and CROs of all sizes are currently managing more than 2,000… https://t.co/AliVArh6Pc Bioclinica (2 weeks ago) With a modular approach, implementation of a configurable, fully featured #CTMS can be achieved in weeks. Even when… https://t.co/Q0KX7YjYNd Bioclinica (3 weeks ago) © Bioclinica. All Rights reserved. Follow us on...