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Best Practices for Medical Coding with MedDRA

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Wed, Oct 10, 2012 10:00 AM EDT 1 hour Dr. Rodney Lemery

Presenter Information
Dr. Rodney Lemery

Meeting Description: MedDRA is a global dictionary used by companies for regulatory activities. The dictionary, complete with clinically validated terminology, is used to classify adverse event information related to the use of drugs, devices, and other therapies. Coding the data to a standard set of MedDRA terms enables health authorities and the life sciences industry to more readily exchange and analyze data. MedDRA is considered the international standard for adverse event classification. However, while the data volume and standardization capabilities offered by the dictionary can provide significant benefits, the multi-axial design and data specificity can introduce considerable challenges that could lead to the inaccurate classification of data. Join BioPharm Systems' Dr. Rodney Lemery, vice president of safety and pharmacovigilance, for this free one-hour webinar that will explore the best practices for medical coding using MedDRA.

Wednesday, October 10, 2012 @: 7:00 a.m. US Pacific time 8:00 a.m. US Mountain time 9:00 a.m. US Central time 10:00 a.m. US Eastern time 15:00 UK time 16:00 Central European time

Dr. Rodney Lemery specializes in the implementation, support, and development of software used in the collection, management, and analysis of clinical data. His accomplishments as vice president of safety and pharmacovigilance at BioPharm Systems include the management of numerous clinical application implementation projects. In addition to his expertise in clinical and safety applications, Rodney is able to navigate between the technical and clinical worlds with ease due to his complementary educational background in epidemiology. He also holds a parttime professorship in the School of Health Sciences at Walden University, which solidifies his ability to lead global safety implementations at BioPharm Systems. Prior to joining the company in 2000, Rodney worked at Pfizer.

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