Webvent

SCRS Resource Guide Network

Sites, Sponsors, CROs: Discover the solutions your clinical research teams need with SCRS.

Complion

eRegulatory and Document Management Platform for Clinical Research Sites

Complion
Header

Complion is a flexible, enterprise platform that enables clinical research sites to centralize and manage regulatory and trial documentation across their institution. Complion removes walls between physicians, administrators and staff by intelligently providing secure access to the right document when they need it. Leading site,s hospitals, health systems, academic medical centers and cancer centers around the country use Complion’s Part 11 platform to go streamline operations and improve regulatory compliance.

Documents 

  • Texas Cardiology Research Department Transforms Document Access, Fuels Productivity

    How Complion Helped a Texas Cardiovascular Research Department Reach New Levels of Efficiency Case Study - STCC Feature Image.pngSouth Texas Cardiovascular Consultants, PLLC (STCC) is a top performing, multi-site health system serving four different cardiology locations in the San Antonio area for over 20 years. Driven to uphold their reputation of providing exceptional patient care along with the highest standards in quality and accuracy, the STCC research department realized that their current paper-based process was slowing them down. They needed to improve the way they were managing regulatory documentation. So when they decided to look f... More »

    Texas Cardiology Research Department Tra...
  • CenterWatch: Regulatory Compliance an Increasing Burden on Sites

    Increased staff time, materials, storage eroding site operating profit The increasing number and complexity of clinical trials has impacted investigative sites in several key areas, including the need to pre-screen larger patient pools, collect more personalized data and perform more time-consuming and complex tasks related to regulatory compliance. While there is agreement that the regulatory compliance burden is high, few initiatives have been launched to measure the direct impact on sites, until now. In this feature article, CenterWatch shares the results of a one-of-a-kind assessment of over 160 investigative sites to understand the exten... More »

    CenterWatch: Regulatory Compliance an In...
  • More eRegulatory Experiences: Embracing a Paperless Process for Your Site

    Embracing a Paperless Process.pngWhile your research site may be working in the shadow of a growing mountain of paper documents and regulatory binders, the prospect of transitioning to an electronic document management system can be daunting. “More eRegulatory Experiences: Embracing a Paperless Process” presents insight from two professionals on the process of moving from paper-based systems to the Complion document management platform. In the article, Dustin Caldwell of OptiMed Research and Neal Surasky of Chesapeake Research Group share the details of the decisions made and obstacles encountered as they severed their tethers to... More »

    More eRegulatory Experiences: Embracing...
  • Steps to Paperless Research Sites: Creating Certified Copies & More

    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" presents insight and expertise from Betsy Fallen, a regulatory and clinical process consultant, on using information technology to tame the paper beast that threatens efficiency and productivity at clinical research sites. Learn valuable tips and how-to steps to help your site transform to digital, including: Printing and Scanning - If a born... More »

    Steps to Paperless Research Sites: Creat...
News: Insights 
  • Protecting Clinical Research Documents From Natural Disasters October 23, 2017 10:48am

    Flooding in Houston. Wildfires in Sonoma. Utter devastation in San Juan. Natural disaster has dominated recent headlines, providing a sobering reminder of just how susceptible we are to the power of nature. Watching the news coverage of people struggling to rebuild lives, homes, and businesses, I find myself wondering if it is even possible to be prepared for such incredible destruction. There are limitations to how much you can protect yourself and your property, and given the level of destruct...
    View this post

  • Tough decisions? See into your eRegulatory future at 2017 Global Site Solutions Summit September 12, 2017 12:43pm

    In life and in business, so many tough decisions would be so much easier to make if you only had the ability to see into the future. But in the real world, the best you can do is to draw on the experience of others who have faced similar critical decisions, learned what works and what doesn’t, and applied those lessons to shape your decision. For most sites the transition to an eRegulatory system is not a matter of if, but when. Fortunately, you have a unique opportunity to draw on the experi...
    View this post

  • Q&A from "Best Practices for Participant Safety: Assessment Documentation and Reporting of Adverse Events" August 18, 2017 10:10am

    The following was provided by the audience question and answer session that was part of the Complion webinar, “Best Practices for Participant Safety: Assessment, Documentation & Reporting of Adverse Events,” featuring Elizabeth Ness, MS, BSN, RN at the Center for Cancer Research, NCI, Ilana Logvinov, RN, MSN, CCRP at Mayo Clinic College of Medicine, and Yolanda McKinney, RN, BSN, CCRC at the Center for Cancer Research, NCI.
    View this post

  • Q&A from Document Management Success: A Guide to Part 11 System Validation August 2, 2017 3:03pm

    The following is based on the Question and Answer portion of “Document Management Success: A Guide to Part 11 System Validation,” a Complion webcast featuring Michelle Grienauer, JD, MPH, Senior Regulatory Attorney at Kinetiq, and Cristina Ferrazzano Yaussy, MPH, CCRP, VP of Professional Services, Complion, Inc. The webinar explored what clinical research sites should know about validating eRegulatory and document management systems. 366 individuals from the clinical research industry atte...
    View this post

  • Complion to Participate in 9th Annual AACI Clinical Research Initiative Meeting July 7, 2017 10:26am

    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 documen...
    View this post

  • How a Texas Cardiovascular Research Department Reached New Levels of Efficiency July 5, 2017 4:38pm

    It’s an increasingly common occurrence at clinical research sites, that moment of realization that the organization is choking on paper. A blizzard of documents and a mountain of bulging folders crushing efficiency and slowing processes to the point that a fleeting thought about a splash of lighter fluid and a well-placed match might pass through the mind of a harried site executive. Cooler heads prevail, of course, and far less incendiary solutions are readily available. Complion has been...
    View this post

Web Site: www.complion.com 

Information

  • Complion
    1621 Euclid Avenue, Suite 2150
    Cleveland, Ohio 44115
    United States
    Map It »
    www.complion.com
  • Events3
  • Documents4
  • News6
  • Last UpdatedOctober 20, 2017 1:11pm EDT

Connect

Contact

  • Rick Arlow
    Rick Arlow

    Founder & CEO
    Complion
    Cleveland, Ohio