Clinical Trial Protocol Amendment Summary

An increased need for specimens of reliable and consistent quality for research purposes requires the development of standardized… (More)

means. If they are copied by any means, the facility will be given 24–48 hours to redact proprietary information from the records… (More)

Canada and the United States have enjoyed vigorous population growth since the early 1980s. Although mortality is slightly higher… (More)

This document, developed by the Rule Interchange Format (RIF) Working Group, specifies how a RIF document can be combined with… (More)

Executive Summary The deliverable D2.1 is the first step towards the definition of a bootstrapping mechanism that implements the… (More)

Executive Summary In this deliverable we provide a revised version of the SerWorks architecture presented in the previous… (More)

This document, developed by the Rule Interchange Format (RIF) Working Group, specifies how a RIF document can be combined with… (More)

In this document we present the status of the work in several topics researched in the BIONETS WP3.2. We illustrate the BIONETS… (More)

Sections 12, 13, and 14 in the second version are new, and the numbering of the other sections has changed accordingly. We have… (More)