In this free webinar, the featured speakers will explain how to design a protocol that allows for decentralized trial elements and key considerations for incorporating virtual services and technologies. Attendees will learn about best practices for data reconciliation, vendor payments and management of integrated technologies.
TORONTO (PRWEB) May 26, 2020
As drug development sponsors are incorporating patient-centric elements into their traditional clinical trial designs, there are several factors to consider during the study planning phase. Whether using telemedicine, mobile nursing services, laboratory support, patient service centers, investigational product management, or a combination of these elements, it is important to develop an operational strategy that allows for flexibility and accounts for complete oversight of each connection point between patients, service providers and the sponsor.
Join this educational webinar to learn best practices for designing a customizable protocol centered around leveraging technology to reduce patient and site burden, streamline data collection and endpoint analysis and optimize study design to support study continuity. Through lessons learned during the global pandemic, the speakers will discuss how to quickly accommodate today’s current studies to function in a decentralized model.
This webinar will also discuss lessons learned for planning ahead to seamlessly apply this approach for future trials. By walking through several real-life examples and providing innovative solutions to traditional schedule of assessments to create operationally sound decentralized clinical trials, the speakers will share insights for operational planning, management of integrated technologies and change management to better equip sponsors with the tools and resources to design a more flexible and resilient protocol focused on patient-centric solutions.
Join Susan Foose, Associate Director, Decentralized Clinical Trials, Covance, Cristina Green, Executive Director, Decentralized Clinical Trials, Covance and Jane Myles, Director, Decentralized Trials Implementation, Covance in a live webinar on Wednesday, June 3, 2020 at 10am EDT (3pm BST/UK).
For more information or to register for this event, visit Decentralized Clinical Trials: Best Practices for Designing a Flexible, Resilient Protocol.
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
For the original version on PRWeb visit: https://www.prweb.com/releases/decentralized_clinical_trials_best_practices_for_designing_a_flexible_resilient_protocol_upcoming_webinar_hosted_by_xtalks/prweb17146064.htm