This document provides an overview of a bug tracking system. It discusses that bug tracking systems can automatically assign bugs to experts based on their experience, maintain a history of resolved bugs to avoid duplicate work, and reduce the time and costs of troubleshooting. The document also summarizes the key modules of a bug tracking system including administration, management, development, testing, and reporting. It outlines how these modules interact and describes strategies to improve bug tracking systems by making them more tool-centric, information-centric, process-centric, and user-centric.
COMBINING REUSABLE TEST CASES AND CONTINUOUS SECURITY TESTING FOR REDUCING WE...ijseajournal
In network communication age, information technology is being at the continuous and rapid evolution
process. Network access equipment, information system and Web Apps must rapidly and continuously update to meet the user interested requirements. Major challenge of Web Apps frequent changes is the security of user personal data and transactions information. Vulnerability scanning and penetration testing are the routine methods to improve the security of Web App. However, these two ways not only timeconsuming, but also require too many resources. For coping the continuous changes, in the limited resources, security testing not only need to be timely completed, but also should concern testing quality. Otherwise, every change mainte nance cannot avoid to cause the security risk of new version App. Based on reusable test cases, this paper proposes the continuous security testing procedure (CSTP), using test cases reusability to increase security test efficiency. In Web Apps maintenance process of limited resources, CSTP
can timely handle security testing and quickly identify Web Apps vulnerabilities and defects. Assisting Apps maintainer effectively repair security defects and concretely improve the security of user personal data and transaction information
What do hospital beds, blood pressure cuffs, dosimeters, and pacemakers all have in common? They are all medical devices with software that regulates their functionality in a way that contributes to Basic Safety or Essential Performance. With the FDA reporting that the rate of medical device recalls between 2002 and 2012 increased by 100% – where software design failures are the most common reason for the recalls – it’s no wonder IEC 62304 has been implemented. Its implementation, however, has medical device manufacturers asking questions about if, when and under what circumstances the standard is required.
This article explains what IEC 62304 is, when medical devices must comply with it and how IEC 62304 compliance is assessed.
Review Paper on Recovery of Data during Software FaultAM Publications
In this paper here we will discuss different types of technique that are used for recovery of data during
software fault. The major objective of this paper to specify recovery technique that are used during software and
hardware fault.
COMBINING REUSABLE TEST CASES AND CONTINUOUS SECURITY TESTING FOR REDUCING WE...ijseajournal
In network communication age, information technology is being at the continuous and rapid evolution
process. Network access equipment, information system and Web Apps must rapidly and continuously update to meet the user interested requirements. Major challenge of Web Apps frequent changes is the security of user personal data and transactions information. Vulnerability scanning and penetration testing are the routine methods to improve the security of Web App. However, these two ways not only timeconsuming, but also require too many resources. For coping the continuous changes, in the limited resources, security testing not only need to be timely completed, but also should concern testing quality. Otherwise, every change mainte nance cannot avoid to cause the security risk of new version App. Based on reusable test cases, this paper proposes the continuous security testing procedure (CSTP), using test cases reusability to increase security test efficiency. In Web Apps maintenance process of limited resources, CSTP
can timely handle security testing and quickly identify Web Apps vulnerabilities and defects. Assisting Apps maintainer effectively repair security defects and concretely improve the security of user personal data and transaction information
What do hospital beds, blood pressure cuffs, dosimeters, and pacemakers all have in common? They are all medical devices with software that regulates their functionality in a way that contributes to Basic Safety or Essential Performance. With the FDA reporting that the rate of medical device recalls between 2002 and 2012 increased by 100% – where software design failures are the most common reason for the recalls – it’s no wonder IEC 62304 has been implemented. Its implementation, however, has medical device manufacturers asking questions about if, when and under what circumstances the standard is required.
This article explains what IEC 62304 is, when medical devices must comply with it and how IEC 62304 compliance is assessed.
Review Paper on Recovery of Data during Software FaultAM Publications
In this paper here we will discuss different types of technique that are used for recovery of data during
software fault. The major objective of this paper to specify recovery technique that are used during software and
hardware fault.
General Principals Of Software Validationstaciemarotta
This guidance outlines general validation principles that the Food and Drug Administration (FDA)
considers to be applicable to the validation of medical device software or the validation of software
used to design, develop, or manufacture medical devices. This final guidance document, Version 2.0,
supersedes the draft document, General Principles of Software Validation, Version 1.1, dated June
9, 1997.
A STUDY OF FORMULATION OF SOFTWARE TEST METRICS FOR INTERNET BASED APPLICATIONSecij
The continuous use of the internet for day to day operations by businesses man, private sector and
government has created a great demand for internet applications. In such kind of application web
server/application server plays vital role. One of the techniques is to test the functionality of web
applications affect user session data received from the web servers. This technique automatically generates
test cases on the behalf of user profiles. The contribution of this paper is the internet application of concept
analysis for clustering user sessions has been reduced. We have completely automated the process from
user session receive and also reduction through replay. In this paper we propose a concept analysis for
internet application and also present a tool Ranorex for the same. In order to execute test case we have a
model for data retrieval. Web application is using in different areas like, medical, insurance, banking etc.
This is chapter 2 of ISTQB Advance Test Manager certification. This presentation helps aspirants understand and prepare the content of the certification.
PROPOSING AUTOMATED REGRESSION SUITE USING OPEN SOURCE TOOLS FOR A HEALTH CAR...ijseajournal
Regression testing is very important for the delivery of high quality product. It helps to simulate a suite of critical test cases periodically and helps to identify if introduction of any new features or any source code change has adversely affected the software quality or functionality. As a result, regression testing cannot be ignored from the software testing life cycle (STLC). But just doing a regression testing cannot be beneficial until it is accompanied by automation testing. Automated regression suite not only saves time and cost by re-running test scripts again and again but it also provide the confidence that all the critical test cases has been covered, providing more confidence in the quality of the product and increasing the ability to meet schedules. IT has an ability to explore the whole software every day without requiring much of manual effort. Current software is going through continuous development which requires testing again and again to check if new feature implementation has affected the existing functionality. In addition to this, it is facing issue in validation of the installation at client site and requires availability of testers to check the critical functionality of the software manually. This paper came up with the solution of creating automated regression suite for the software. The current research will provide guidelines to the future researchers on how to create an automated regression suite for any web application using open source tools.
This presentation was delivered as a webinar for FDAnews, delving into software, medical devices and managing risk with 21 CFR Part 11 and IEC 62304. It provides:
• A historical backdrop of IEC 62304
• An overview of IEC 62304
• Implementing IEC 62304
• Common pitfalls to avoid
Analytical and other equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability.
AN ANALYSIS OF SOFTWARE REQUIREMENTS SPECIFICATION CHARACTERISTICS IN REGULAT...ijseajournal
Requirements Engineering is the set of activities involved in creation, managing, documenting, and maintaining a requirements’ set for a product. Engineering involves the use of systematic repeatability techniques to ensure that the Software Requirements are complete, consistent, valid, and verifiable. Software Requirements Specification is an organized process oriented toward defining, documenting and maintaining requirements throughout the development life cycle. Many authors suggest that requirements should always focus their claims on what the software product needs to address, without specifying how to implement them. However, the detail of Software Requirements is influenced by several factors such as: organizational thinking; existing specification standards; and regulatory needs. This work fits exactly with regulatory needs, where the characteristics of Software Requirements Specification in Regulated Environments such as aeronautics, railways and medical are presented and explored. This paper presents and analysis of software requirements specification characteristics in regulated environments. The four characteristics identified are: consistency (internal and external), unambiguity, verifiability, and traceability. The paper also describes the three standards used in these regulated environments (RTCA DO-178C, IEC 62279 and IEC 62304) and examines their similarities and differences from a Requirements Specification standpoint. The similarities and differences will be used to address a future requirements framework universal process that can be configured to address each standard by the usage of Software Process Lines.
APPLICATION WHITELISTING: APPROACHES AND CHALLENGESIJCSEIT Journal
Malware is a continuously evolving problem for enterprise networks and home computers. Even security
aware users using updated security solutions fall into trap of zero day attacks. Moreover, blacklisting
based solutions suffer from problems of false positives and false negatives. From here, idea of Application
whitelisting was coined among security vendors and various solutions were evolved with same underlying
technology idea. This paper provides the details about design and implementation approaches and
discusses challenges while developing an effective whitelisting solution.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
General Principals Of Software Validationstaciemarotta
This guidance outlines general validation principles that the Food and Drug Administration (FDA)
considers to be applicable to the validation of medical device software or the validation of software
used to design, develop, or manufacture medical devices. This final guidance document, Version 2.0,
supersedes the draft document, General Principles of Software Validation, Version 1.1, dated June
9, 1997.
A STUDY OF FORMULATION OF SOFTWARE TEST METRICS FOR INTERNET BASED APPLICATIONSecij
The continuous use of the internet for day to day operations by businesses man, private sector and
government has created a great demand for internet applications. In such kind of application web
server/application server plays vital role. One of the techniques is to test the functionality of web
applications affect user session data received from the web servers. This technique automatically generates
test cases on the behalf of user profiles. The contribution of this paper is the internet application of concept
analysis for clustering user sessions has been reduced. We have completely automated the process from
user session receive and also reduction through replay. In this paper we propose a concept analysis for
internet application and also present a tool Ranorex for the same. In order to execute test case we have a
model for data retrieval. Web application is using in different areas like, medical, insurance, banking etc.
This is chapter 2 of ISTQB Advance Test Manager certification. This presentation helps aspirants understand and prepare the content of the certification.
PROPOSING AUTOMATED REGRESSION SUITE USING OPEN SOURCE TOOLS FOR A HEALTH CAR...ijseajournal
Regression testing is very important for the delivery of high quality product. It helps to simulate a suite of critical test cases periodically and helps to identify if introduction of any new features or any source code change has adversely affected the software quality or functionality. As a result, regression testing cannot be ignored from the software testing life cycle (STLC). But just doing a regression testing cannot be beneficial until it is accompanied by automation testing. Automated regression suite not only saves time and cost by re-running test scripts again and again but it also provide the confidence that all the critical test cases has been covered, providing more confidence in the quality of the product and increasing the ability to meet schedules. IT has an ability to explore the whole software every day without requiring much of manual effort. Current software is going through continuous development which requires testing again and again to check if new feature implementation has affected the existing functionality. In addition to this, it is facing issue in validation of the installation at client site and requires availability of testers to check the critical functionality of the software manually. This paper came up with the solution of creating automated regression suite for the software. The current research will provide guidelines to the future researchers on how to create an automated regression suite for any web application using open source tools.
This presentation was delivered as a webinar for FDAnews, delving into software, medical devices and managing risk with 21 CFR Part 11 and IEC 62304. It provides:
• A historical backdrop of IEC 62304
• An overview of IEC 62304
• Implementing IEC 62304
• Common pitfalls to avoid
Analytical and other equipment should be qualified and computer systems should be validated to demonstrate suitability for the intended use. Electronic records must comply with FDA Part 11 and EU/PICS GMP Annex 11 requirements to ensure data integrity, security and availability.
AN ANALYSIS OF SOFTWARE REQUIREMENTS SPECIFICATION CHARACTERISTICS IN REGULAT...ijseajournal
Requirements Engineering is the set of activities involved in creation, managing, documenting, and maintaining a requirements’ set for a product. Engineering involves the use of systematic repeatability techniques to ensure that the Software Requirements are complete, consistent, valid, and verifiable. Software Requirements Specification is an organized process oriented toward defining, documenting and maintaining requirements throughout the development life cycle. Many authors suggest that requirements should always focus their claims on what the software product needs to address, without specifying how to implement them. However, the detail of Software Requirements is influenced by several factors such as: organizational thinking; existing specification standards; and regulatory needs. This work fits exactly with regulatory needs, where the characteristics of Software Requirements Specification in Regulated Environments such as aeronautics, railways and medical are presented and explored. This paper presents and analysis of software requirements specification characteristics in regulated environments. The four characteristics identified are: consistency (internal and external), unambiguity, verifiability, and traceability. The paper also describes the three standards used in these regulated environments (RTCA DO-178C, IEC 62279 and IEC 62304) and examines their similarities and differences from a Requirements Specification standpoint. The similarities and differences will be used to address a future requirements framework universal process that can be configured to address each standard by the usage of Software Process Lines.
APPLICATION WHITELISTING: APPROACHES AND CHALLENGESIJCSEIT Journal
Malware is a continuously evolving problem for enterprise networks and home computers. Even security
aware users using updated security solutions fall into trap of zero day attacks. Moreover, blacklisting
based solutions suffer from problems of false positives and false negatives. From here, idea of Application
whitelisting was coined among security vendors and various solutions were evolved with same underlying
technology idea. This paper provides the details about design and implementation approaches and
discusses challenges while developing an effective whitelisting solution.
Process and Regulated Processes Software Validation ElementsArta Doci
Medical device manufacturers operate in a competitive marketplace with increasing end-user demands for features and usability and in a highly regulated environment.
Regulatory bodies look for evidence that medical devices are developed under a structured, quality-oriented development process. By following software validation and verification best practices, one can not only increase the likelihood that they will meet their compliance goals, they can also enhance developer productivity.
Bug Tracking System is a web-based application that is designed to help quality assurance and programmers keep track of reported software bugs in their work. Bugs will be assigned to a person with a bug id, flag, description, project name.
Technology Used
Operating System : Windows XP or above
User Interface : HTML, CSS
Client-side Scripting : PHP
Back End : MySQL
Web Server : Apache Tomcat 7.0.22
IDE : NetBeans 7.1
Online dating system management project report.pdfKamal Acharya
The objective of our project is to develop an application that offers online dating services where individuals or users can find and contact each other over the internet to arrange a date usually with the objective of developing a romantic, personal and sexual relationship.
Users of an online dating service would currently provide personal information, to enable them to search the service provider's database for other individuals. Members use grade other members set, such as age range, gender and location.
Bug triage means to transfer a new bug to expertise developer. The manual bug triage is opulent in time
and poor in accuracy, there is a need to automatize the bug triage process. In order to automate the bug triage
process, text classification techniques are applied using stopword removal and stemming. In our proposed work
we have used NB-Classifiers to predict the developers. The data reduction techniques like instance selection
and keyword selection are used to obtain bug report and words. This will help the system to predict only those
developers who are expertise in solving the assigned bug. We will also provide the change of status of bug
report i.e. if the bug is solved then the bug report will be updated. If a particular developer fails to solve the bug
then the bug will go back to another developer.
A Review on Software Fault Detection and Prevention Mechanism in Software Dev...iosrjce
IOSR Journal of Computer Engineering (IOSR-JCE) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of computer engineering and its applications. The journal welcomes publications of high quality papers on theoretical developments and practical applications in computer technology. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Bug Tracking System is a web-based application that is designed to help quality assurance and programmers keep track of reported software bugs in their work. Bugs will be assigned to a person with a bug id, flag, description, project name.
Operating System : Windows XP or above
User Interface : HTML, CSS
Client-side Scripting : PHP
Back End : MySQL
Web Server : Apache Tomcat 7.0.22
IDE : NetBeans 7.1
Similar to IRJET- A Review on Bug Tracking System (20)
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Hierarchical Digital Twin of a Naval Power SystemKerry Sado
A hierarchical digital twin of a Naval DC power system has been developed and experimentally verified. Similar to other state-of-the-art digital twins, this technology creates a digital replica of the physical system executed in real-time or faster, which can modify hardware controls. However, its advantage stems from distributing computational efforts by utilizing a hierarchical structure composed of lower-level digital twin blocks and a higher-level system digital twin. Each digital twin block is associated with a physical subsystem of the hardware and communicates with a singular system digital twin, which creates a system-level response. By extracting information from each level of the hierarchy, power system controls of the hardware were reconfigured autonomously. This hierarchical digital twin development offers several advantages over other digital twins, particularly in the field of naval power systems. The hierarchical structure allows for greater computational efficiency and scalability while the ability to autonomously reconfigure hardware controls offers increased flexibility and responsiveness. The hierarchical decomposition and models utilized were well aligned with the physical twin, as indicated by the maximum deviations between the developed digital twin hierarchy and the hardware.
Saudi Arabia stands as a titan in the global energy landscape, renowned for its abundant oil and gas resources. It's the largest exporter of petroleum and holds some of the world's most significant reserves. Let's delve into the top 10 oil and gas projects shaping Saudi Arabia's energy future in 2024.
About
Indigenized remote control interface card suitable for MAFI system CCR equipment. Compatible for IDM8000 CCR. Backplane mounted serial and TCP/Ethernet communication module for CCR remote access. IDM 8000 CCR remote control on serial and TCP protocol.
• Remote control: Parallel or serial interface.
• Compatible with MAFI CCR system.
• Compatible with IDM8000 CCR.
• Compatible with Backplane mount serial communication.
• Compatible with commercial and Defence aviation CCR system.
• Remote control system for accessing CCR and allied system over serial or TCP.
• Indigenized local Support/presence in India.
• Easy in configuration using DIP switches.
Technical Specifications
Indigenized remote control interface card suitable for MAFI system CCR equipment. Compatible for IDM8000 CCR. Backplane mounted serial and TCP/Ethernet communication module for CCR remote access. IDM 8000 CCR remote control on serial and TCP protocol.
Key Features
Indigenized remote control interface card suitable for MAFI system CCR equipment. Compatible for IDM8000 CCR. Backplane mounted serial and TCP/Ethernet communication module for CCR remote access. IDM 8000 CCR remote control on serial and TCP protocol.
• Remote control: Parallel or serial interface
• Compatible with MAFI CCR system
• Copatiable with IDM8000 CCR
• Compatible with Backplane mount serial communication.
• Compatible with commercial and Defence aviation CCR system.
• Remote control system for accessing CCR and allied system over serial or TCP.
• Indigenized local Support/presence in India.
Application
• Remote control: Parallel or serial interface.
• Compatible with MAFI CCR system.
• Compatible with IDM8000 CCR.
• Compatible with Backplane mount serial communication.
• Compatible with commercial and Defence aviation CCR system.
• Remote control system for accessing CCR and allied system over serial or TCP.
• Indigenized local Support/presence in India.
• Easy in configuration using DIP switches.
Explore the innovative world of trenchless pipe repair with our comprehensive guide, "The Benefits and Techniques of Trenchless Pipe Repair." This document delves into the modern methods of repairing underground pipes without the need for extensive excavation, highlighting the numerous advantages and the latest techniques used in the industry.
Learn about the cost savings, reduced environmental impact, and minimal disruption associated with trenchless technology. Discover detailed explanations of popular techniques such as pipe bursting, cured-in-place pipe (CIPP) lining, and directional drilling. Understand how these methods can be applied to various types of infrastructure, from residential plumbing to large-scale municipal systems.
Ideal for homeowners, contractors, engineers, and anyone interested in modern plumbing solutions, this guide provides valuable insights into why trenchless pipe repair is becoming the preferred choice for pipe rehabilitation. Stay informed about the latest advancements and best practices in the field.