For the past several years, Complion has hosted a monthly educational webinar series featuring thought leaders in the clinical research industry. We’re proud to say each session has attracted an overwhelming number of attendees, and many have indicated the information provided in the webinars has been invaluable in their work. The series is so popular we regularly receive inquiries about the topic of the next webinar and when it will take place.
Unfortunately, we’ve had to pause our monthly webinar series due to the current challenges presented by the COVID-19 pandemic. Our primary goal at this time is to focus on supporting our clinical research customers by doing all we can to make their work not only easier, but possible, so they can maintain their focus on clinical trials.
During the pandemic, the burden of work has become even heavier and more pressing for the clinical research industry. Some of our customers have had to hold operations, while others are involved in COVID-19 vaccine trials. Many are trying to continue trials that can’t afford to be stopped amid strict practices of distancing and quarantining. In addition, many research sites have staff working remotely or are required to work with patients remotely during the pandemic. Regardless, important documents still need managed, updated, shared and signed.
To that end, the Complion team continues to work diligently to provide its site-centric eRegulatory solution to Research Sites, Sponsors and CROs. For Sites, the objective is to ensure simpler storage, retrieval and sharing of regulatory documentation as well as compliant e-signatures no matter where staff is located. For Sponsors and CROs, the software platform enables cost containment and improved quality of site monitoring during the COVID-19 pandemic and going forward.
Rest assured, we’ll soon resume our educational webinar series with timely and thought-provoking industry topics presented by a new lineup of research thought leaders.
Until then we wish you all continued health and safety.
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Are you looking for a partner to help you simplify management of clinical trial documentation while improving site efficiency and compliance? Discover how Complion can help.