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Complion

eRegulatory and Document Management Platform for Clinical Research Sites

Complion
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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 Blog 
  • Rowing in the Same Direction: Integrating eRegulatory and CTMS Systems November 13, 2017 9:17am

    In summer months you can look down from one of the bridges spanning the Cuyahoga River here in Cleveland, Ohio to see rowing teams seated in slender rowing shells, slicing through the murky water. In each shell team members pull on their oars, propelling the sleek craft with remarkable speed and efficiency. Of course, that speed is possible only when everyone rows in cadence, and in the same direction. That same level of coordination and integration is absolutely essential for the technologies...
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  • Bio-Optronics and Complion Announce Integration to Unify Best-in-Class CTMS and eRegulatory Solutions for Clinical Research Organizations November 12, 2017 11:31am

    November 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...
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  • Electronic Signatures in Clinical Research: Lifting the Paper Curse October 31, 2017 10:23am

    Scenes of someone being relentlessly pursued, perhaps by zombies, vampires, flying sharks, or some combination of any or all of the above, are common on TV during Halloween season. And that’s ok. But somewhat similar scenes are also playing out in the halls of research facilities as research nurses or regulatory coordinators attempt to chase down busy Primary Investigators (PIs) whose signatures are needed on essential documents. Staff members set up ambushes, pen and documents in hand, waitin...
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  • 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...
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  • 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...
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  • 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.
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Web Site: www.complion.com 

Information

  • Complion
    1621 Euclid Avenue, Suite 2150
    Cleveland, Ohio 44115
    United States
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    www.complion.com
  • Events3
  • Documents4
  • News6
  • Last UpdatedJanuary 22, 2018 3:27am EST

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Contact

  • Rick Arlow
    Rick Arlow

    Founder & CEO
    Complion
    Cleveland, Ohio