ClinPhone Exhibits its Clinical Trial Technology Solutions at 42nd DIA Annual Meeting
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.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
