I am looking forward to presenting this workshop at MAGI West to take our attendees beyond just the basics and apply advanced GCP concepts.
Seattle, WA (PRWEB) October 21, 2014
Quorum Review IRB, the industry leader in central IRB services, announces Director of Regulatory Affairs and General Counsel Linda Coleman, JD, CIP, CHC, CHRC, as a presenter at MAGI’s 2014 Clinical Research Conference – West. This year MAGI West will be held at the Fairmont in San Francisco, CA, November 9-12, 2014.
Ms. Coleman will lead the program, “Good Clinical Practice: Advanced Workshop,” which covers important GCP topics, informed consent topics, investigator oversight, and inspection findings. Other presenters at the workshop will include Phil Coran, Director of Medidata Solutions, and Gloria Cosgrove, the former Senior Director of Compliance and Inspection Management at Regeneron Pharmaceuticals. Attendees are encouraged to bring their own questions and real world experiences to engage the speakers on GCP topics. The presentation takes place Sunday, November 9th from 9:30 a.m. to 4:45 p.m. Ms. Coleman adds, “I am looking forward to presenting this workshop at MAGI West to take our attendees beyond just the basics and apply advanced GCP concepts.”
Ms. Coleman has over a decade of legal expertise in clinical trial research and regulatory oversight. She joined Quorum Review in 2007 as the Director of Regulatory Affairs and today continues to serve that role in addition to the role of General Counsel, which she assumed early in 2011. In April 2012, Ms. Coleman was honored by Puget Sound Business Journal as “Outstanding Corporate Counsel for a Small Business” (<1000 employees), recognizing her legal expertise in research matters and contribution to education.
MAGI’s 2014 Clinical Research Conference is one of the most visible events in the clinical research industry. The conference offers an exceptional networking environment with a large variety of sessions and workshops that provide practical tips in a coherent program for operations, regulatory compliance, contracts and budgets. More information about the 2014 conference is available on the MAGI website.
About Quorum Review IRB
Quorum Review is an independent institutional review board fully accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP), and has been providing ethics review of human clinical research since 1992. Quorum oversees research in accordance with U.S. and Canadian human subject research protection regulations and guidelines set forth by the International Committee on Harmonisation (ICH), and principles of the Belmont Report.
Quorum’s best-in-class service and support includes 15 Board meetings each week, plus expedited review, 24-hour site review turnaround, 36-hour amendment review turnaround, a secure web portal, and SmartForms for online submissions. Quorum’s service offerings include full study review in the US, as well as internationally; a specialized Phase I team; institution-specific support; and efficient processes for minimal risk studies.