Trial Trends™

Gut Feelings: Navigating Life with Crohn's, We're excited to announce the release of our latest episode of the Trial Trends™ Podcast! In this episode, our host, Libbi Rickenbacher shares a deeply personal conversation with her co-host, Kathleen Greenough. Kathleen shares her journey as a new patient with IBD, offering heartfelt insights into the challenges and triumphs she has experienced...thus far. Her story provides a unique and touching perspective that truly resonates. Through Kathleen's narrative, this episode beautifully highlights the transformative power of sharing personal experiences. Tune in now to join this inspiring conversation!

- How fully digitalized, real-time temperature monitoring through integration with Randomization and Trial Supply Management (RTSM), leads to better oversight, quicker decision-making, a reduction of human error and increased patient safety - Showcase the application of in-transit monitoring of a Highly Advanced, Personalized and temperature sensitive drug, requiring real-time tracking of temperature, light, tilt, and location - Showcase how automated real-time communication solutions between on-site logger technology and the RTSM system transform drug supply management and oversight, whilst reducing the administrative burden on site users

In this part 2, your host Libbi Rickenbacher and guest Siobhan McKenna-Power dive into the world of RTSM development, shedding light on the critical role of the sponsor-vendor partnership. Join them as they explore how prioritizing the patient experience throughout the RTSM development process is paramount. Libbi and Siobhan emphasize the significance of fostering a true partnership between sponsors and vendors, enabling a focus on the sites and ultimately, the patient, from inception to execution. Through collaboration, stakeholders can ensure that the design and implementation of RTSM systems align with the needs and experiences of those participating in clinical trials. Moreover, this episode delves into the crucial aspect of data security and management within RTSM development. Ensuring compliance with regulatory standards and safeguarding sensitive information are imperative in maintaining trust and integrity in clinical research.

In part 1 of this episode, Libbi and Siobhan delve into the escalating intricacies of clinical trials, shedding light on the challenges and solutions within the realm of Randomization and Trial Supply Management (RTSM) build for clinical trial protocols. As the pharmaceutical and biotech industries evolve, so does the demand for adaptive and nuanced approaches to address the growing complexity in trial designs. The conversation unfolds as they explore the delicate nuances involved in tailoring the RTSM build directly to the specific needs of the protocol. Siobhan, drawing from her extensive experience, emphasizes the critical role of having a proficient team of RTSM experts. Together, they dissect the importance of this expertise in supporting end-users and, ultimately, ensuring the well-being of patients throughout the clinical trial journey.

In this podcast, dive into the ever-evolving landscape of clinical trials as we reflect on the overall trends of 2023 and cast our gaze forward into 2024. Join our hosts as they dissect the latest methodologies, technological advancements, and regulatory shifts shaping the future of clinical research and explore what tomorrow may have in store.