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CHI & Barnett International Announces its Second Annual Clinical Auditing Forum

Ensuring Audit Readiness and GCP Compliance across Clinical Research Functions

 
PRLog - Apr. 11, 2012 - NEEDHAM, MASS. – April 11, 2012 – Regulatory agencies’ changing focus and expanding expectations regarding GCP compliance will be addressed at the Second Annual Clinical Auditing Forum. This two day event takes place June 6-7, 2012 in Boston, MA. Attendees can expect presentations on auditing best practices, strategies, and techniques to ensure that solid GCP compliance and scientific and ethical standards are maintained throughout the conduct of clinical trials. Sessions will be focused on developing and strengthening auditing programs, implementing proven techniques for audit planning, and ultimately ensuring clinical research compliance through strategic approaches to clinical quality assurance. FDA and international regulatory agency expectations and recent inspection trends will be discussed. Speakers will present real-world examples of risk-based approaches to auditing sites, systems, and providers. For more information, please visit http://www.clinicaltrialsummit.com/Clinical-Auditing-Forum/

Speakers Include:  (partial listing)

-  Doreen McGirl, Senior Manager, Global Clinical Compliance, Merck

- Kelly Willenberg, BSN, M.B.A., CHRC, President, Synergism, LLC

- Anna DeMarinis, Principal, The DeMarinis Group, LLC; former FDA Consumer Safety Officer, Health Sciences Administrator, and Policy Analyst

- Swati Tendolkar, Program Manager, Global System Quality Assurance, Janssen R&D, a Johnson & Johnson company

- Rod Thorell, Director, Quality Management & Compliance, Quality Management & Compliance, PHT Corporation

- Johanna L. Stamates, RN, MA, CCRC, CHRC, Executive Director, Regulatory Support and Quality Assurance, University of Miami

- Jan Holladay Pierre, MPH, Manager of Clinical Quality Assurance, DynPort Vaccine Company LLC

- Laura Paolinelli, Senior Quality Assurance Associate, Quality Assurance, Westat

- Kimberly Dorsch, CCRP, CRCP, Director, Clinical Research, Sentara Medical Group

- Marie Jackson, Ph.D., M.B.A., Director, Clinical Research Administration & Services, City of Hope

- Hope Senechal, B.Sc., CCRA, Clinical Research Auditor, Administration, Ottawa Hospital Research Institute

For more information, or to register, please visit http://www.clinicaltrialsummit.com/Clinical-Auditing-Forum/.  Register by April 27 to save up to $200!

About Cambridge Healthtech Institute (www.chicorporate.com)
Cambridge Healthtech Institute (CHI) is the preeminent life science network for leading researchers and business experts from top pharmaceutical, biotech and academic organizations. CHI’s portfolio of products includes Cambridge Healthtech Institute Conferences, Insight Pharma Reports, Barnett International, Cambridge Marketing Consultants, Cambridge Meeting Planners and Cambridge Healthtech’s Media Group, which includes numerous e-newsletters as well as Bio-IT World magazine.

Founded in 1992, Cambridge Healthtech Institute strives to develop quality information sources that provide valuable new insights and competing points of view while offering balanced coverage of the latest developments. Basic research related to commercial implications is covered, with heavy emphasis placed on end-user insights into new products and technology as well as coverage on the strategy behind the business.

Contact:
Tracey Fielding
Marketing Manager
Cambridge Healthtech Institute
tfielding@healthtech.com

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Contact Email:
***@healthtech.com
Source:Cambridge Healthtech Institute
Phone:781.972.5400
Zip:02494
City/Town:Needham - Massachusetts - United States
Industry:Government, Medical, Research
Tags:Clinical Auditing, GCP compliance, clinical trials, fda
Shortcut:prlog.org/11845983
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