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

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Bio-Optronics, creator of Clinical Conductor CTMS, is one of the fastest growing healthcare workflow optimization software and services companies, dedicated to positively impacting the lives of patients and providers. Recognized for providing the comprehensive functionality required to recruit effectively, optimize billing, maintain research compliance, extract actionable business insight and maximize profitability, Clinical Conductor is also integrated with the major clinical systems, eliminating double entry issues. Used by more research sites than any other system, Clinical Conductor CTMS simplifies and standardizes complex clinical research processes and finances for professionals managing and conducting clinical trials, helping our users run the world’s best research and increasing the chances of being the chosen site for each new opportunity.

Click here for free access to The Ultimate Guide to Clinical Trial Software!


Also visit www.bio-optronics.com or follow @BioOptronics on Twitter or LinkedIn 

Products 

  • Clinical Conductor CTMS

    Clinical Conductor CTMS is the only clinical trial management system with strong financial and compliance capabilities that is designed to accommodate the unique needs of your organization across multiple sites and countries. Run the world’s best research.


    More Information » bit.ly/2Tkjj8i

    Clinical Conductor CTMS
Documents 

Documents

QPS Miami Research Case Study
January 10, 2018 11:44am

Documents

CRS Case Study
January 10, 2018 11:44am

Documents

Integration with Complion
January 10, 2018 11:47am

News: Bio-Optronics 
  • Making the Case for eReg Sponsor Support  May 28, 2020 4:14pm

    eRegulatory software is a game changer for clinical research sites in terms of digitizing regulatory management.  Replacing bulky binders with easy-to-navigate resources accessible by any computer connected to the site system saves time, enables multi-site efficiencies, and ensures accuracy of the data. But as you consider an investment in eReg, you should look beyond its […]
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  • Remote Trial Management: Keeping the Human Touch May 26, 2020 8:56am

    While remote trial management capabilities might have seemed unnecessary even just a few months ago, there’s no denying that clinical trial organizations need to incorporate these tools sooner rather than later. And while it’s critical to prepare your sites with a strong plan and deploy the right technologies that support remote trial management, don’t overlook […]
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  • Decentralized Trial Management Checklist May 21, 2020 9:09am

    Strong eClinical platforms, sponsor support, and current event demands have made decentralized trial management more accessible to clinical research sites than ever. CRO and site management need to anticipate what practices and technologies will enable decentralized trial management for their work. Here is a checklist of critical considerations as sites seek to begin or enhance […]
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  • COVID-19 Resources for Clinical Research Organizations April 24, 2020 2:33pm

    During the COVID-19 pandemic, many clinical research professionals have been trying to understand HIPAA and clinical trial regulations, as well as the impact on protocol management. In order to provide support to the clinical research community, below are several guidance documents related to HIPPA and clinical trial regulations: Human Subject Protection & Federal Regulations of […]
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  • FDA Inspections Made Easier April 16, 2020 1:54pm

    Although you never know when one might happen, preparing for FDA inspections is necessary for all clinical research sites. Early and comprehensive preparation for an inevitable inspection is perhaps the best predictor of a successful audit. The best way to prepare for an audit is to transition your paper-based systems to digital. Sites that shift […]
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  • How Can I Minimize CRA Site Visit Cost & Disruption? April 13, 2020 8:50am

    Successfully managing Clinical Research Associate (CRA) site visits is a critical part of any clinical research organization. CRA monitoring, while a mandatory and non-negotiable part of managing and monitoring a clinical trial, has a very real impact on the daily work of your site. Therefore, minimizing daily work disruption, optimizing resources spent on site visits, […]
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Information

  • Bio-Optronics
    1890 South Winton Road
    Rochester, New York 14618
    United States
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    bio-optronics.com
  • Products1
  • Events3
  • Videos1
  • Documents3
  • News6
  • Last UpdatedMay 29, 2020 12:27am EDT

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Contacts

  • Michael Bonavilla
    Michael Bonavilla

    Director, Business Development
    Bio-Optronics, Inc.
    Charlotte, South Carolina


  • Katie Gaiek
    Katie Gaiek

    Sales Executive
    Bio-Optronics
    Rochester, New York