qc2 will be in booth 1516 at the DIA 21st Annual EuroMeeting in Berlin, Germany on March 23-25, 2009, and in booth 1000 at the DIA 45th Annual Meeting in San Diego, CA on June 21-25, 2009.
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Joe Mardesich and Lee Bertram, Principal Consultants for qc2, conducted a training course for IBC-Asia in both Shanghai and Singapore on May 17-22, 2007.
The course was titled
GCPs in Practice: Ensuring Compliant Trials and Preparing for FDA Inspections.
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David Lieck, a Senior Consultant with qc2, wrote an article for the February 2007 issue of the Journal of Clinical Research Best Practices titled,
Institutional Review Board Safety Reporting Policies: Are Changes for the Better?
Please click here to read the article.
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Joe Mardesich spoke at the RAPS 2006 Annual Conference and Exhibition. The session was titled,
Managing Clinical Trials and Preparing for a Bioresearch Inspection.
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Joe Mardesich and Lee Bertram conducted two training courses for IBC-Asia in Bangkok, Thailand on February 21-24, 2006.
The courses were
SOPs for Clinical Research and
Quality Assurance & Preparing for FDA Inspections in Clinical Trials.
Lee and Joe have also twice conducted these courses in Singapore.
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Joe Mardesich spoke at the Drug Information Association (DIA) 10th Annual Computer Validation and 3rd Annual IT Conference in Williamsburg, VA on September 13, 2005. His topic was
A Practical Approach to Evaluating Clinical Electronic Data Capture Systems.
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Lee Bertram spoke at the January 18, 2005 meeting of the San Diego Chapter of the Association of Clinical Research Professionals. The topic of the discussion was
How to Prepare your Clinical Investigative Site for an Audit.
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Joe Mardesich wrote an article for the July 2004 issue of DIA Forum (Vol. 40 Issue 3). The title of the article is
EDC Systems - A Seamless Transition.
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David Lieck spoke at the Barnett International Preparing for Clinical Audits and Inspections Conference in Philadelphia, PA on May 6, 2004. The title of his session was
Investigational Product Accountability and Reconciliation at Investigative Sites: FDA Findings in Recent Warning Letters.
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Lee Bertram spoke at the Pacific Region Clinical Supllies (PARCS) meeting in San Diego, CA on April 16, 2004.
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David Lieck and Jason Bertram, Senior Project Manager / Auditor with qc2, wrote an article titled
Drug Accountability at the Investigative Site for the March 2002 issue of Applied Clinical Trials.
