PAREXEL Launches RTSM Mobile App
Boston, MA – PAREXEL International Corporation, a leading global biopharmaceutical services provider, today launched a mobile app for the ClinPhone RTSM (randomization and trial supply management) service. The app is designed to enhance clinical trial supply management processes, increase patient safety, and improve the chain of custody record for clinical supplies.
Using built-in barcode scanning capabilities, clinical trial site staff, including principal investigators (PIs), study nurses, and clinical research associates (CRAs), can utilize the app to streamline common clinical trial responsibilities. Tasks including confirming correct treatment allocation, dispensing to patients, and processing of medicinal product returns can now be managed more efficiently, reducing time and human errors.
“Clinical trials management is often hampered by administrative supply-related tasks at site locations. Simplifying systems and processes and removing manual data entry can save staff time and increase patient safety,” said Ken Faulkner, Corporate Vice President, PAREXEL Informatics. “Our mobile app is the latest extension of the ClinPhone RTSM service, further demonstrating our commitment to simplifying the drug development journey through the innovative application of social, mobile, analytic, and cloud technologies.”
PAREXEL’s ClinPhone RTSM service has been deployed on over 3,700 studies and more than 2.5 million patients, with the largest of those studies randomizing and supplying more than 60,000 patients. The ClinPhone RTSM mobile app is available worldwide for use on Android and iOS platforms. For more details, please visit: https://www.parexel.com/solutions/informatics/randomization-and-trial-supply- management/rtsm-mobile-app.
About PAREXEL International
PAREXEL International Corporation is a leading global biopharmaceutical services company, providing a broad range of expertise-based clinical research, consulting, medical communications, and technology solutions and services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, and reimbursement. PAREXEL Informatics provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL has offices in 85 locations in 51 countries around the world, and had approximately 19,625 employees in the first quarter. For more information about PAREXEL International visit www.PAREXEL.com.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
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.
Landmark Phase III Trial Shows Keytruda Significantly Improves Event-Free Survival in LA-HNSCC
April 28th 2025Interim KEYNOTE-689 trial data show that perioperative Keytruda significantly lowers the risk of disease progression or recurrence in resectable, locally advanced head and neck squamous cell carcinoma, marking the first major clinical advance for this patient population in more than two decades.
