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Application of Metadata Repository and Master Data Management in Clinical Trial and Drug Safety

Application of Metadata Repository and Master Data Management in Clinical Trial and Drug Safety
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Author(s): Chandrakant Ekkirala (Cognizant Technologies Limited, India)
Copyright: 2016
Pages: 14
Source title: Software Innovations in Clinical Drug Development and Safety
Source Author(s)/Editor(s): Partha Chakraborty (Cognizant Technology Solutions, India) and Amit Nagal (GVK Bioscience, India)
DOI: 10.4018/978-1-4666-8726-4.ch003

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Abstract

This chapter talks about metadata repository, and master data management in clinical trial and drug safety. The chapter begins with the definition of metadata repository and gives an explanation around the same, It talks about a well designed metadata repository and the characteristics associated with the same. A brief around why we need metadata and the reasons for the using the same has also been mentioned. The benefits of a well structured metadata repository was also mentioned in detail. The chapter then gives a detailed explanation on master data management and the usage of MDM in clinical trials. MDM solutions for clinical trials management is also explained in detail.

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