ClinPhone will be exhibiting its complete range of clinical trial technology services at the 42nd DIA Annual Meeting.
Technologies being showcased at booth # 1009 include ClinPhone's TrialWorks®, ePRO (Electronic Patient Reported Outcomes), ClinPhone's integration suite for Electronic Data Capture Systems (EDC) and Clinical Trial Management Software (CTMS), Randomization and Trial Supply Management services. ClinPhone will also be launching an exciting new service which is to be announced during the show.
Showcasing at booth # 1009 will be ClinPhone's TrialWorks®, our enterprise-level, globally scalable Web-based CTMS. This user-friendly system is used by more pharmaceutical, biotech and CRO organizations than any other CTMS, and supports our clients in the day-to-day tracking, reporting and management of regulatory and clinical information. Two ancillary components will also be available: the Universal Transfer Tool (UTT), used to import relevant data from other clinical trial technologies, and our new TrialWorks® Monitoring Module (TMM), which allows monitors/CRAs to work offline and to automatically create monitoring reports. TrialWorks®, the UTT, and the TMM collectively enable ClinPhone to offer its customers the "total" clinical trial management solution.
ClinPhone is also promoting its ePRO solution at DIA which delivers real-time, cost-effective electronic patient reported outcomes data. The 21 CFR part 11 compliant technology eliminates concerns over limitations on data quality and integrity of paper diaries and questionnaires by using the company's powerful Interactive Voice Response (IVR) system. ClinPhone ePRO is simple and intuitive to use, offering unparalleled diary compliance, study site access to patient data and simultaneous application in an unlimited number of languages and countries.
Also being demonstrated at booth # 1009 is ClinPhone's integration technology for EDC and CTMS systems. This offers customers a flexible interface between their EDC and/or CTMS software and ClinPhone's real-time trial management systems. This application creates an environment where critical randomization and dispensing data are seamlessly shared between systems in real-time. Unlike other integration solutions, ClinPhone's enables data to originate in either system and also offers protocol-specific integration touch-points.
Stay current in clinical research with Applied Clinical Trials, providing expert insights, regulatory updates, and practical strategies for successful clinical trial design and execution.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Managing Side Effects and Dosing in Off-Label GLP-1 Use with Help from Real-World Evidence
July 18th 2025Shipra Patel, global therapeutic area section head, endocrinology, global head, pediatrics, Parexel, explains how real-world data is helping researchers navigate gastrointestinal side effects, dose flexibility, and long-term tolerability in off-label GLP-1 use.
Anselamimab Misses Primary Endpoint in Phase III CARES Trials for AL Amyloidosis
July 17th 2025In the Phase III CARES trials, anselamimab did not meet the primary endpoint for advanced-stage AL amyloidosis, but a prespecified subgroup analysis revealed meaningful improvements in survival and cardiovascular outcomes.