Sentence examples for further on this implementation from inspiring English sources

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Further on, this implementation is independent of the platform, being able to map to any available FPGA.

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"Plus customers have the option to get the latest functionalities without going through further on-site implementation".

This paper presents the inspiration of a conceptual model capable to originate an effective, scalable e-Government ontology and further on, the implementation of an ontology-based repository for designing, modelling and even reengineering of governmental services; pilot tested in the Greek Government.

Participant 2, Vendor A Before formal procurement had started, when deciding on a system, frequent contact with potential vendors and other organisations that were further on in the implementation journey was seen as helpful.

Given the consistent benefit of feedback demonstrated, this supports further research on this topic and implementation of structured intraoperative feedback initiatives.

Interviews were designed to elicit further detail on implementation strategies and processes, and why these hospitals were able to implement changes related to their urinary catheter use.

The population of next generation ( P^{ G + 1)} ) is created as follows (Selection): Further details on implementation of DE to the design of water distribution are available in Suribabu (2010).

For further details on implementation and algorithms, see the Supplementary Material.

Due to scant evidence in the current literature, further research on implementation and effectiveness of CCDSS is required.

This could be seen as a limitation, but it does not reduce the validity of the results, as the objective of analysis was to determine if an end-user was choosing a framework for a particular innovation would the frameworks targeting this innovation be the most suitable, or would a framework, created for the implementation of a different innovation, add further details on implementation concepts.

Further discussion on implementation is required; for example, it should be explored whether the reanalysis of study data with the aim of generating information on the approved patient population could already be routinely provided by the regulatory process (for example, in European public assessment reports).

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