Navigating the Regulatory Maze to Enable Trial Continuity with Digital Solutions, Upcoming Webinar Hosted by Xtalks
TORONTO (PRWEB) June 08, 2020 -- The scale of the challenges those of us responsible for clinical development have faced and continue to deal with during the COVID-19 pandemic has been unprecedented and complex. Across our industry, everyone responsible for the conduct of clinical trials has been forced to make sound decisions, fast.
Digital solutions have seen wider acceptance to maintain clinical trial continuity. While traditionally there has been slow uptake for these technology-based solutions in clinical trials, primarily due to a lack of legal, patient and data privacy, and regulatory frameworks, stakeholders have recognized their key suitability for supporting clinical trial continuity during the pandemic.
To date, regulatory authorities have repeatedly advised that emergency measures being facilitated during the pandemic are only interim measures and that things will essentially revert to business as usual once COVID-19 is under control. However, industry experts recognize the circumstances of the COVID-19 pandemic create important opportunities to change and improve the way clinical trials can be run going forward.
This webinar will discuss how digital solutions, including decentralized trials, can improve the trial experience for patients, maintain regulatory compliance, increase efficiency and speed delivery of reliable data. The speakers will explain how the successful adoption of a digital framework that safeguards patient safety and produces accurate and reliable data during the pandemic helps fuel the needed agency buy-in to progress this promising approach beyond the pandemic. They will also discuss common themes of current regulatory authority guidelines and important considerations to enable you to successfully navigate the regulatory landscape when planning to introduce digital solutions to clinical trials.
Join PPD regulatory affairs subject matter experts Christina Cocciardo, Marci Aderiye and Ilse-Maria Nolan in a live webinar on Wednesday, 24 June, 2020 at 11 a.m. EDT (4 p.m. BST/UK).
For more information or to register for this event, visit Navigating the Regulatory Maze to Enable Trial Continuity with Digital Solutions.
ABOUT XTALKS
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.
To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/
Ayesha Rashid, Xtalks, +1 (416) 977-6555 x 272, [email protected]
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