Quorum Review IRB and Kinetiq to sponsor, exhibit, and participate at the MAGI West clinical research conference, including presenting three informative sessions.
(SAN FRANCISCO, CA): Leaders of Quorum Review IRB and Kinetiq, the consulting and technology division of Quorum, will present on emerging trends in clinical research next week at the Model Agreements and Guidelines International (MAGI) 2017 Clinical Research Conference West November 12-15, at the Fairmont Hotel in San Francisco.
On the first day of the conference, Mitchell Parrish, Kinetiq Vice President of Regulatory Affairs, will present a master class on “Good Clinical Practice and Inspection Readiness.” This all-day workshop on November 12 will include an interactive format to evaluate key changes to the Common Rule and suggest considerations for implementation in to existing human research protection programs.
James Riddle, Vice President of Client Services for Kinetiq, will co-present on emerging issues in human subjects protection. This hard-hitting session previews emerging hot topics that impact regulatory compliance for clinical research. This session will be presented on November 13 at 11:30 a.m.
Michelle Grienauer, Senior Regulatory Attorney for Kinetiq, will participate in an insightful panel discussion on the regulatory fine points to unveil what the rules really say. This session will occur on November 13 at 1:30 p.m.
Visit Quorum and Kinetiq at the Quorum booth to participate in a survey about electronic consenting—anyone who participates will receive a gift card. Or visit us at Laurel Court in the Fairmont Hotel as we host an informal drink reception on November 12 at 6:30 p.m.
Quorum Review IRB is the largest and most preferred central IRB. As the first name in streamlined, service-centered independent ethics and regulatory review, the Quorum difference is One-Touch Collaboration™. Your research benefits from an outstanding service experience, a single point of contact, one study startup timeline, and a true single board review. Beyond traditional institutional review board services, Quorum offerings include single IRB (sIRB) services for institutions and the world’s first IRB-integrated electronic informed consent solution: Q Consent™. Kinetiq, the consulting and technology division of Quorum, moves your research forward with services that enhance and optimize the clinical research process.
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