Chinese Journal of Pharmacovigilance ›› 2015, Vol. 12 ›› Issue (6): 341-346.

Previous Articles     Next Articles

Study on Application of Data Organization and Common Data Model of the Observational Medical Outcomes Partnership in US

WANG Ling   

  1. Center for Drug Reevaluation, CFDA, Beijing 100045, China
  • Received:2015-05-04 Online:2015-06-08 Published:2015-07-27

Abstract: Objective To provide thought and references for the promotion of ADR monitoring in China, suggestions on the secondary use of observational data for maximizing the benefit and minimizing the risk of drug use. Methods The data organization and access models of the Observational Medical Outcomes Partnership in US and the Common Data Model were studied and analyzed. Results and Conclusion The establishment and implementation of OMOP has obvious characteristics. In order to use existing multiple observational healthcare databases for active drug safety and benefit monitoring, the critical factor and the basis on the technical levels are the construction, improvement and unification of the medical information standards. The CDM design, development and evaluation can provide good thought and references for secondary use of observational data and active drug safety surveillance by establishing partnership and using a variety of data sources in China.

Key words: observational data, secondary use, data model, active surveillance

CLC Number: