Insights Blog

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 experience of panel of professionals who have completed that transformation at the 2017 Global Site Solutions Summit, taking place October 6-8, 2017 in Boca Raton, FL.

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.

Complion 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.

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.

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.

Complion, the industry-leading document management and workflow platform for clinical research sites, will be exhibiting at MAGI's 2016 West Coast Clinical Research Conference in Las Vegas, Nevada from October 23–26.

The Complion team will be at the Planet Hollywood Resort & Hotel to connect with the research community and share best practices for managing clinical trial documents in a manner that improves efficiency and oversight.

Complion, the industry-leading document management and workflow platform for clinical research sites, will be exhibiting at the 2016 Global Site Solutions Summit in Boca Raton, Florida from October 13–16.

The Complion team will be at booth 504 to connect with the research community by sharing knowledge and experiences on regulatory and operational areas with attendees.