Advertisement
MINNEAPOLIS, Aug. 20 /PRNewswire-USNewswire/ -- The Health Care Compliance Association (HCCA) announced today it will hold its annual Research Compliance Conference on October 18-20, 2009, at the Hyatt Regency Minneapolis, Minneapolis, MN. This is an essential conference for anyone working in medical research today -- whether it be for a sponsor, a research site, or clinicians who conduct research.
Advertisement
Hot Topics
This year's Research Conference will address a number of critical issues including
Expert Faculty
Hear directly from industry experts and compliance and ethics professionals who will provide practical perspectives for handling research compliance risks. Conference speakers who are working in today's leading research institutions including: University of Chicago Medical Center, University of North Carolina at Chapel Hill, UCLA Medical Sciences, Catholic Healthcare West, HCA, UK Healthcare of the University of Kentucky, Allina Hospitals & Clinics, University of California, University of Virginia, and Rush University Medical Center will address a variety of critical issues faced by organizations conducting clinical trials and working in medical research.
Conference Details and Registration
For the complete agenda use the following link to the brochure http://www.hcca-info.org/StaticContent/09ResearchComp_brochure.pdf.
About the HCCA
The Health Care Compliance Association (HCCA), established in 1996 and headquartered in Minneapolis, MN, is a non-profit professional membership organization made up of compliance and ethics professionals working in the health care industry. HCCA is dedicated to improving the quality of compliance.
Its mission: HCCA exists to champion ethical practice and compliance standards and to provide the necessary resources for ethics and compliance professionals and others who share these principles. Visit the HCCA Web site at www.hcca-info.org. Tel: 888/580-8373.
-- Government Review: ORI and OHRP Compliance Oversight: Recent Cases and Initiatives -- Impact of Medicare developments on clinical research reimbursement -- Overview of clinical research compliance enforcement -- Adverse Events: What Should Be Reported to the IRBs -- Our Bodies? Compliance Challenges and Solutions for Body and Specimen Donation for Research -- Developing a Comprehensive Program for Managing Conflicts of Interest -- Overview of Privacy Requirements and Compliance Issues in International Clinical Trials (European Law, Canadian Law -- and others)
SOURCE Health Care Compliance Association
