Clinical Trial Data and Coding Processes - Sonja Brajovic, M.D., DIA 44th Annual Meeting, Boston, MA, June 2008

Adverse Event Pathway and MedDRA Coding - Sonja Brajovic, M.D., DIA 23rd Annual Clinical Data Management Conference, March 2008

MedDRA Coding Impact on Data Retrieval & Analysis within FDA AERS - Amarilys Vega, M.D., MPH - DIA 43rd Anual Meeting, Atlanta, GA, June 2007

Narrative Writinig for Clinical/Postmarketed Safety Adverse Event Reports - Mark Vieder, R.Ph., DIA 43rd Anual Meeting, Atlanta, GA, June 2007

MedDRA Training - Mark Vieder, R.Ph., DIA 43rd Anual Meeting, Atlanta, GA, June 2007

Utilization of Medication Error Terms within MedDRA - Judith McMeekin, Pharm.D., DIA 43rd Anual Meeting, Atlanta, GA, June 2007

Importance of Data Quality Throughout the Drug Development Lifecycle - Amarilys Vega, M.D., MPH - DIA 22nd Annual Clinical Data Management Conference, March 2007

Medication Errors Surveillance - DIA 42nd Annual Meeting, Philadelphia, PA June 2006 (PDF 256kb)

Mentor-Protégé Approach in Training - DIA 42nd Annual Meeting, Philadelphia, PA June 2006 (PowerPoint 528kb)

Drug Safety Surveillance Process Overview: MedDRA® Application and Challenges From Clinical Trials to Post-Authorisation - 18th DIA Annual Euromeeting (Poster Session) March 2006 (PowerPoint 82.5 kb)

MedDRA® Training: Mentor Protégé Approach & Skills Maintenance Program -18th DIA Annual Euromeeting (Poster Session) March 2006 (PowerPoint 351 kb)

MedDRA® Processing of Adverse Event Reports in ADE Surveillance Systems - 41st DIA Annual Meeting (Poster Session) June 2005 (PowerPoint 82 kb)

Monitoring Drug Safety - 17th DIA Annual Euromeeting (Poster Session) March 2005 (PowerPoint 74 kb)

Establishing a MedDRA® Safety Surveillance Unit -  presented at the "Working With MedDRA^®" symposium, London UK (includes discussion of Legacy Data Conversion) September 99 (PowerPoint 164 kb)

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