Abbie Hosta

Educational Outreach at Complion, a SaaS platform that is transforming the way clinical trial site documentation is created and maintained. Passionate about technology, education, and helping others work more effectively.
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Recent Posts

Meet Complion at ACRP’s Annual Meeting & Expo

Posted by Abbie Hosta on Apr 20, 2017 9:00:11 AM

Complion, the industry-leading regulatory and document management platform for clinical research sites, will be exhibiting the the Association of Clinical Research Professionals (ACRP) Annual Meeting & Expo in Seattle, Washington from April 28-May 1.

The Complion team will be at the Washington State Convention Center to connect with the research community and share best practices for managing clinical trial documents in a manner that improves efficiency and oversight.

The ACRP Meeting & Expo will host over 2,000 clinical research professionals and 100 expert speakers. Attendees get the opportunity to learn from the influencers, innovators and regulators driving change in clinical trial operations. U.S. FDA officials will be onsite during an exclusive ‘FDA Office Hours’ forum and will several educational sessions designed to provide clarity on agency expectations related to CDER BIMO compliance and enforcement, electronic records, eSource data, eConsent, and more.

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Topics: News, Events

Complion Founder Rick Arlow to Co-Host SCRS Webinar

Posted by Abbie Hosta on Apr 10, 2017 11:42:44 AM

Complion Founder and CEO, Rick Arlow, along with Advanced Clinical Trials President, Jeremy Rigby, will host an educational webinar for the Society of Clinical Research Sites (SCRS) on April 25, 2017.

Earn credit for one Contact Hour by attending Embracing a Paperless Process: Best Practices for Regulatory and Document Management. This one-hour webinar will focus on best practices for electronic document management and explore strategies for saving time and money and improving compliance by connecting new eRegulatory and document systems to existing systems.

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Topics: eRegulatory, News, Paperless Clinical Trials, Paperless Research Sites, Document Management

Complion Article Featured in ACRP’s Flagship Journal, Clinical Researcher

Posted by Abbie Hosta on Apr 5, 2017 10:52:17 AM

Complion is honored to have recently published an article in Clinical Researcher, the peer-reviewed flagship publication of the Association of Clinical Research Professionals (ACRP).

Clinical Researcher is published six times a year and features articles on the latest developments across the spectrum of specialty areas in the clinical research enterprise, as well as highlighting valuable insights and resources from columnists, internal and external news sources, and the Association’s partner organizations.

Written by Complion VP of Professional Services Cristina Ferrazzano Yaussy and Oklahoma Heart Hospital Senior Director James Wetzel, Ensuring Compliance with Part 11: A Site's Perspective focuses on best practices for maintaining maximum efficiency while meeting the challenges of Part 11 compliance.

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Topics: News, Compliance, Regulatory Compliance, 21 CFR Part 11

Steps to Paperless Clinical Trials: Creating Certified Copies and More

Posted by Abbie Hosta on Mar 20, 2017 3:13:39 PM

Whether you’ve taken the first steps toward a paperless clinical trial environment, or are still contemplating that very important transformation, you will want to take advantage of a new resource now available from Complion.

Steps to Paperless Clinical Trials: Creating Certified Copies and More, a new Complion feature article, presents insight and expertise from Betsy Fallen on using information technology to tame the paper beast that threatens efficiency and productivity at clinical research sites.

A recognized authority on the role of IT in regulatory and clinical operation and data management, Betsy’s early training as a registered nurse has kept her focus on patient welfare throughout her career. Now a regulatory and clinical process consultant, Betsy spent several years in regulatory and clinical operations with Merck and Co., along the way accumulating expertise in moving clinical trials to paperless environments.

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Topics: Paperless Clinical Trials, Regulatory Compliance, Paperless Research Sites, Certified Copies

The Paperless Research Site: Best Practices for Regulatory and Document Management

Posted by Abbie Hosta on Mar 3, 2017 11:21:21 AM

Have you ever experienced the frustration or uncertainty associated with finding the right protocol or trial document? Does searching through messy binders, cluttered inboxes and separate systems or shared drives slow you down?

Watch this on-demand webinar and learn how to combat this problem. Complion Founder and CEO Rick Arlow, will discuss how an eRegulatory and document system can complement and connect with CTMS and other systems to save time, improve compliance and improve access. Explore best practices for managing documents electronically and learn from real-world experiences at similar sites.

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Topics: eRegulatory, CTMS, Paperless Research Sites