Towards Lightweight Requirements Documentation
نویسندگان
چکیده
منابع مشابه
Towards Lightweight Requirements Documentation
Most requirements management processes and associated tools are designed for document-driven software development and are unlikely to be adopted for the needs of an agile software development team. We discuss how and what can make the traditional requirements documentation a lightweight process, and suitable for user requirements elicitation and analysis. We propose a reference model for requir...
متن کاملMultimedia Product Documentation - User Requirements
The globalisation of industry and the strong dependence of the German machine manufacturers on export has increased the importance of an up-to-date and user-oriented product documentation not only as a cost factor but as a competition factor of strategic importance as well. The use of Multimedia is a promising approach to realize such an improved documentation. This paper presents the results o...
متن کاملSemantic Documentation in Requirements Engineering
Currently, most requirements documents are prepared using desktop text editors. These documents are intended to be used by human readers. In this paper, we discuss the use of semantic annotations in requirements documents, in order to make information regarding links between requirements and other software artifacts, such as other requirements, use cases, classes and test cases, interpretable b...
متن کاملAdaptable Documentation and Traceability of Software Requirements
The current solutions for the Requirement Engineering do not possess support for the inclusion or exclusion, of quality factors and elements to describe specific patterns of requirements as the use cases or forms of a certain project. The lack of that support makes the storage model and description of the static requirements difficult; in other words, those solutions hinder the definition of di...
متن کاملGuideline on the requirements for quality documentation
Keywords Biological product, investigational medicinal product (IMP), clinical trial, quality Guideline on the requirements for quality documentation concerning biological investigational medicinal products in clinical trials
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Software Engineering and Applications
سال: 2010
ISSN: 1945-3116,1945-3124
DOI: 10.4236/jsea.2010.39103