Join Complion at MAGI East

Complion Travels to Boston for MAGI East 2022

Joe Wochna Tradeshows and Events

Complion is excited to be at MAGI’s Clinical Research Hybrid Conference – 2022 East.  This year’s event takes place at the Sheraton Boston Hotel in Boston, Massachusetts.  The conference will continue MAGI’s vision of streamlining clinical research by standardizing best practices for clinical research operations, business and regulatory compliance.

Complion will be at MAGI East

The event will feature over 90 sessions grouped into several tracks including Site Management, Regulatory Compliance, and others.  Conference planners expect more than 600 attendees and will live steam several sessions as well.  This in-person event will comply with local and national safety and health protocols.  Visit the MAGI Event site for details.

As a proud sponsor at this year’s MAGI East, Complion will be on display in the Exhibit Hall (booth #107) that will showcase the latest integrations and capabilities of the pioneering eRegulatory/eISF solution.   Plus visitors to the booth will have a chance to win a Kindle Fire!

Featured Session

Rick Arlow, Complion’s Founder and CEO, will be presenting:  “Lessons Learned: How Top Sites Manage eReg/eISF” on Monday, May 2nd at 2:15pm.  Mr. Arlow will discuss how you can improve study conduct and patient safety so you can quickly and compliantly add more investigators; manage amendments and study changes.

Rick Arlow

Rick Arlow
Complion Founder & CEO

In additional, he will cover how to eliminate unnecessary interaction and redundancy while providing a higher quality and consistent service for your Sponsor and CRO requirements.  Presentation slides will be made available per request.

Several members of the Complion team will be present, representing Leadership, Sales, and Customer Experience.

If you are not able to attend in person, we encourage you to check out www.complion.com for more information or to request a personalized demonstration.

About Complion

Complion is a leading provider of clinical investigator compliance technology for Sites, Sponsors and CROs. The company’s mission is to initiate clinicians on-demand and eliminate the unnecessary burden of document silos, including eISF/eReg, RSDV/R, Site Qualification and Document Exchange. We manage over 20,000 Site Files for 22,000 PIs used in over 50 countries.