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


Industry Leading eRegulatory Platform for Clinical Research Sites


Save time and simplify your regulatory tasks with Complion, the industry’s leading eRegulatory solution designed to make your life easier. 

• Eliminate paper binders
• Collect eSignatures
• Track expirations and outstanding tasks
• Ensure 21 CFR Part 11 Compliance
• Standardize filing and naming conventions
• Simplify remote monitoring

Experience the Complion Difference

• Trusted by 80+ sites to manage over 4,000 studies.
• Accessed by 1400+ monitors from 170+ sponsors and CROs!
• The only system designed to automate repetative tasks
• Best practices and industry standards
• Template policies and SOPs to ensure your long-term success
• Maximize sponsor acceptance and reimbursement
• Largest and most experienced team on the market

Sign up for a free demonstration today!


  • 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 
  • Streamlining Regulatory Processes with eSignatures November 26, 2018 9:43am

    It has been more than 20 years since the FDA established that electronic documents and signatures were trustworthy and acceptable for use in clinical research (so long as they meet 21 CFR Part 11 requirements). In that time, many research organizations have taken the opportunity to free themselves of the struggle to manage mountains of paper and chase down doctors for signatures. But many have yet to make the transition.
    View this post

  • Q&A Follow-up from “What ICH E6(R2) Really Means for Research Sites!” November 13, 2018 2:05pm

    Polaris Compliance Consultants was delighted to present Complion’s October 24th webinar, “What ICH E6(R2) Really Means for Research Sites!” Far more questions were submitted during the webinar than we could address during the Q&A period, so we would like to answer them here. It was interesting to see that most of the questions related to documentation and document retention. That can be a confusing area for study sites. We hope you find these responses helpful.
    View this post

  • Complion to Exhibit at 2018 MAGI West October 19, 2018 9:54am

    Complion, the industry leading eRegulatory platform for clinical research sites, will be speaking and exhibiting at the 2018 MAGI West conference, taking place in San Diego, California October 21-24, 2018. Complion Founder & CEO, Rick Arlow, will be a panelist on the session, ISF/TMF Integration, to share insights on how sites and sponsors can work together to ensure complete and accurate records and streamline regulatory tasks.
    View this post

  • Complion Customer Receives “Exceptional” Rating from National Cancer Institute September 25, 2018 4:38pm

    One of the most rewarding, exciting, and humbling aspects of the work we do here at Complion is that it allows us to engage with organizations that are leading the charge to develop new therapies to treat patients suffering from a range of ailments. Some exciting recent news puts one of our clients into the spotlight. The National Cancer Institute (NCI) has awarded the Robert H. Lurie Comprehensive Cancer Center of Northwestern University the highest possible rating on the competitive renewal o...
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  • Complion to Participate in the 2018 Global Site Solutions Summit September 24, 2018 2:53pm

    Complion, the industry-leading eRegulatory platform for clinical research sites, will be speaking and exhibiting at the 2018 Global Site Solutions Summit, taking place in Boca Raton, Florida on October 12-14, 2018. Complion will be kicking off the summit by inviting site members to Miznar's Monkey Bar on October 11th from 8-11PM. Upon arriving to the Boca Raton Resort, attendees can enjoy wine and artisanal foods while listening to the acoustic sounds of Johnny Champagne or enjoying an outdoor...
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  • eRegulatory Buyer's Guide: A 38-Point Checklist for Choosing the Right Solution August 21, 2018 12:46pm

    Download your at-a-glance guide to choosing an eRegulatory solution. As a research coordinator or administrator, being buried under a mountain of paper files is something that doesn’t have to happen often before the light bulb in your head suddenly glows with the realization that there must be a better way. Light bulbs are clicking on in similar fashion across the industry, and their accumulated illumination is shining on eRegulatory systems. The rate at which organizations are adopting eReg...
    View this post

Web Site: www.complion.com 


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    1621 Euclid Avenue, Suite 2150
    Cleveland, Ohio 44115
    United States
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  • Last UpdatedApril 5, 2020 2:02pm EDT



  • Rick Arlow
    Rick Arlow

    Founder & CEO
    Cleveland, Ohio