Developments, news and strategies for drug development specific to phase I through Phase III global clinical trial management, execution, project management and outsourcing. Go→
News, articles and issues specific to clinical trial practice and implementation at the investigative site level. Go→
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News, developments and strategies for clinical trials conduct in relation to the FDA, EMEA and other global regulatory authorities overseeing the drug development industry. Go→
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ArisGlobal, a provider of solutions to the life sciences industry, has announced agDisclosure™ 3.1, a system that enables sponsors to plan, prepare and manage submissions to multiple registries. agDisclosure is the newest addition to ArisGlobal’s Total Clinical™, a comprehensive platform for clinical research that includes EDC, CTMS, ePRO, medical coding, supply chain management and safety reporting -- all accessed via agWorld™, a central clinical portal. “Clinical trial transparency is an established expectation today and this is being reinforced by regulation in many parts of the world,” commented Mathias Poensgen, product manager at ArisGlobal. “There are many registries and each requires differing data sets with unique business rules based on local regulation. Until standardization is achieved, the entire disclosure process will remain complex. With agDisclosure, sponsors can manage all disclosure activity from a single platform, reusing data sets multiple times while reports, metrics and dashboards give users insight into the worldwide status of their registries.” · Flexible database structure with business rules adaptable to future registry requirements and new fields added without coding efforts. · Import of data from any CTMS, including ArisGlobal’s agClinical™.
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