Topics will include, but are not limited to data integrity, key stakeholders, trial design, operational considerations, essential infrastructure and insights into both the role and value these types of trials will have in the future.
TORONTO (PRWEB) July 30, 2020
Companies exploring the use of hybrid or decentralized trials during this new era of drug development are encouraged to join this webinar for an interactive panel session featuring leaders from across the industry to learn from their direct experience.
During this webinar, panelists will explore ways in which hybrid and decentralized trials have altered traditional clinical pathways and the new landscape that sponsors, sites and patients must navigate as a result of the COVID-19 pandemic. The panelists will also highlight the challenges and opportunities with transitioning to a hybrid or decentralized trial strategy and what they would recommend for those planning to do the same. Topics will include, but are not limited to data integrity, key stakeholders, trial design, operational considerations, essential infrastructure and insights into both the role and value these types of trials will have in the future.
Join our expert panel, Niklas Morton, senior vice president, digital services, PPD, Brittany Erana, vice president, PPD® Digital, Triniette Mitchell, director, clinical data integrity and technology, Takeda Pharmaceuticals, and Michelle Longmire, MD, co-founder, CEO, Medable in a live webinar on Thursday, 20 August, 2020 at 10:00 a.m. EDT (3pm BST/UK).
For more information or to register for this event, visit The Transformation of Clinical Trial Design & Operations: A Panel Discussion on COVID-19 as a Catalyst for Decentralized Trials.
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