Insights Blog

University of Cincinnati Cancer Institute Abstract Awarded 1st Place for 10th Annual AACI CRI Meeting

Posted by Abbie Hosta on Jul 3, 2018 2:39:48 PM

As recently announced by the Association of American Cancer Institutes, an abstract created in a collaboration by the University of Cincinnati Cancer Institute and Complion has been awarded first place by the AACI CRI steering committee and selected to be presented in formal sessions at the 10th Annual AACI Clinical Research Initiative Meeting, July 11-12, in Chicago.

Selected from among a record 68 submissions, the winning entry, “Building a Strong Foundation: How Leveraging Cross Collaboration Can Improve Standardization and Adoption of an eRegulatory Solution,” was written by Trisha Wise-Draper, MD, PhD; Justin Osborne; Benjamin Quast, MBA, CCRP; Emily Werff, all from the University of Cincinnati Cancer Institute, and Michael Hurley, MBA, of Complion.

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Topics: eRegulatory, News, Regulatory Compliance, Document Management, Standardization, Cancer Center

Bio-Optronics and Complion Announce Integration to Unify Best-in-Class CTMS and eRegulatory Solutions for Clinical Research Organizations

Posted by Complion on Nov 12, 2017 11:31:02 AM

Complion_BioOptronics_Partner.pngNovember 11, 2017 – ROCHESTER, NY – Bio-Optronics, the makers of the market leader Clinical Conductor Clinical Trial Management System (CTMS), and Complion, the powerful eRegulatory and document management platform for sites, have partnered to integrate their best-in-class solutions to deliver an industry-leading solution for research organizations.

The companies are building upon their long-standing commitment to meet customer needs and develop innovative solutions to empower investigative sites to run the world’s best research. This integration introduces a highly robust application suite, enabling research organizations to operate efficiently and profitably, while maintaining compliance with 21 CFR Part 11, HIPAA, and Good Clinical Practice (GCP).

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Topics: eRegulatory, News, CTMS, Regulatory Compliance, Billing Compliance, Document Management

Complion to Participate in 9th Annual AACI Clinical Research Initiative Meeting

Posted by Complion on Jul 7, 2017 10:26:27 AM

Complion, the industry-leading regulatory and document management platform for clinical research sites, will be speaking and exhibiting at the 9th Annual AACI Clinical Research Initiative Meeting from July 12-13, 2017.

Complion Founder and CEO, Rick Arlow, will be conducting a vendor presentation on Thursday, July 13, entitled, Going Paperless: Managing Regulatory & Clinical Trial Documents in Complion. Mr. Arlow will discuss best practices for managing regulatory and clinical trial documentation in cancer centers. In particular, he will explore document and information management from a research enterprise perspective, defining how systems and teams can (and should) function together to centralize information and drive performance.

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Topics: News, Events

Complion to Speak at 2017 MAGI East Conference

Posted by Abbie Hosta on May 15, 2017 8:29:53 AM

Untitled design-456548-edited.pngComplion VP of Professional Services, Cristina Ferrazzano Yaussy MPH, CCRP, along with Stephanie Berger, Salima Dhanji, MPH, and Angelo Termine, BS, MSM, MBA, CCRC/A, CRCP, will be presenting Part 2 of the Master Class workshop series entitled, Site Management Innovation on Sunday, May 21, 2017 at the MAGI Clinical Research Conference in Philadelphia, PA.

During this session, the panel will present their perspective innovative ideas to address long-standing and emerging challenges, and work together to identify and develop best practices in three areas: leveraging metrics to drive performance, innovative site management structures & practices, and information management systems.

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Topics: News, Events

Complion to Exhibit at AAHRPP Annual Conference

Posted by Complion on May 9, 2017 9:37:21 AM

 

Complion will be exhibiting at the 2017 AAHRPP Annual Conference in Detroit Michigan from May 10th - 11th. Our team will be at booth 112 to connect with the research community and share knowledge.

Complion's 21 CFR Part 11 compliant platform helps accredited and non-accredited sites, hospitals, health systems, cancer centers and academic medical centers save time and focus on medical advancements while maintaining safety and compliance.

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Topics: News, Events

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.

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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

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Complion provides clinical research sites and their sponsors with a software platform to enable secure, compliant and efficient management of documents and administrative tasks. We would love to hear from you with any questions about our Insights blog or to learn more about our software platform.

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