The document discusses quality assurance and software testing. It defines quality assurance as activities designed to ensure production meets requirements and standards. Software quality assurance means monitoring processes to ensure quality. Key components of quality assurance are software testing, quality control, and software configuration management. Software testing investigates quality by providing stakeholders information about the product under test.
Software Testing : Quality Assurance (QA) v/s Quality Control (QC) : Definition | Focus | Comparison | Scope | Approach
Some of the most confusing terminologies of software testing
Quality assurance is a wide ranging concept covering all matters that individually and collectively influence the quality of product.
It is the arrangements made with the object of ensuring that pharmaceutical products are of the quality required for the intended use.
Assurance of product quality is derived from careful attention of factors including selection of quality parts and materials, adequate product and process design, control of the process, and in-process and end-product testing.
Software Testing : Quality Assurance (QA) v/s Quality Control (QC) : Definition | Focus | Comparison | Scope | Approach
Some of the most confusing terminologies of software testing
Quality assurance is a wide ranging concept covering all matters that individually and collectively influence the quality of product.
It is the arrangements made with the object of ensuring that pharmaceutical products are of the quality required for the intended use.
Assurance of product quality is derived from careful attention of factors including selection of quality parts and materials, adequate product and process design, control of the process, and in-process and end-product testing.
009 what are the systems validation protocol methods at atl 05 28-2015atlmarketing
If your product must meet the requirements of FDA cGMP, 21 CFR 210, 211, 820, ISO-9000, ISO-13485, or MDD/93/42/EEC (for the CE Mark), there are three very critical elements you must have to be in regulatory compliance. First, you must have a sound and strong Quality Management System (QMS). This is an expression of WHAT you do (your quality policies and structure). Second, you must have reliable Standard Operating Procedures (SOP’s). These are expressions of HOW YOU DO THINGS.
Missing in the above two items is an expression of HOW WELL YOU DO WHAT YOU DO? This is where you must establish your “Systems Validation Protocol” (SVP). Your SVP is an expression of how well your system is working (for example, this can be expressed in overall product conformance percentage or in defects per million for your various products). The SVP is a living and continuous document based on your quality records. The ATL White Paper “What Are The Systems Validation Protocol Methods At ATL?” is our attempt to share with you a sound approach to Systems Validation and the various protocols that you can use.
Get trained on practical aspects of FDA process validation, equipment qualification, Data analysis, statistical tools for Process Quality Management, more.
This PPT contains defination of control of qulity, measures of quality, unit of measures of quality, self-control,the sensor, image of spreadsheet to explain sensor, image of measures drivers, difference between classic control and self-control etc in brief.
009 what are the systems validation protocol methods at atl 05 28-2015atlmarketing
If your product must meet the requirements of FDA cGMP, 21 CFR 210, 211, 820, ISO-9000, ISO-13485, or MDD/93/42/EEC (for the CE Mark), there are three very critical elements you must have to be in regulatory compliance. First, you must have a sound and strong Quality Management System (QMS). This is an expression of WHAT you do (your quality policies and structure). Second, you must have reliable Standard Operating Procedures (SOP’s). These are expressions of HOW YOU DO THINGS.
Missing in the above two items is an expression of HOW WELL YOU DO WHAT YOU DO? This is where you must establish your “Systems Validation Protocol” (SVP). Your SVP is an expression of how well your system is working (for example, this can be expressed in overall product conformance percentage or in defects per million for your various products). The SVP is a living and continuous document based on your quality records. The ATL White Paper “What Are The Systems Validation Protocol Methods At ATL?” is our attempt to share with you a sound approach to Systems Validation and the various protocols that you can use.
Get trained on practical aspects of FDA process validation, equipment qualification, Data analysis, statistical tools for Process Quality Management, more.
This PPT contains defination of control of qulity, measures of quality, unit of measures of quality, self-control,the sensor, image of spreadsheet to explain sensor, image of measures drivers, difference between classic control and self-control etc in brief.
Roca, a popular name in the world of sanitary products has emerged as a trusted brand in recent years owing to its high-end product range. With an array of products at its disposal, Roca offers tailor-made solutions that can suit the need of every bathroom. The durability of all its products is ensured by the fine-quality construction and the global presence in over 135 counties speaks volumes about their credibility too. The revolutionary technology used in Roca has made it a world leader in bathroom products and its innovative designs have made their own mark.
Clean Energy Ministerial - Digital Media Year+ in ReviewValerie Riedel
This presentation reviews the performance of the Clean Energy Ministerial's digital media platforms - an email newsletter; a large website; and social media accounts on LinkedIn, twitter, Facebook, and YouTube. The review is a "year in review - plus," covering the 15 months from the launch of the twitter, FB, and LinkedIn pages in Feb. 2013 to the conclusion of the CEM's annual meeting in May 2014.
The presentation reviews goals and objectives, defines potential measurements for reporting on each, presents highlights from a detailed review of these measures, and suggests next steps to build on successes and address key challenges.
Quality assurance (QA) is a way of preventing mistakes or defects in manufactured products and avoiding problems when delivering solutions or services to customers.
Quality control (QC), is a process by which entities review the quality of all factors involved in production.
All software engineering works toward a single goal: to produce high-quality software
Software quality assurance (SQA) is an umbrella activity that is applied throughout the software process.
The SQA activities and technical review help us in ensuring the quality of software product
2. QUALITY ASSURANCE
• Quality assurance is a way of preventing mistakes or defects in
manufactured products and avoiding problems when delivering solutions
or services to customers; which ISO 9000 defines as "part
of quality management focused on providing confidence
that quality requirements will be fulfilled".
• Quality assurance is a system of activities designed to ensure
production that meets pre-established requirements and standards.
3. SOFTWARE QUALITY ASSURANCE
• Software quality assurance (SQA) means monitoring
the software engineering processes and methods used to ensure
quality.
• It is a planned effort to ensure that a software product fulfills
criteria and has additional attributes specific to the product.
4. COMPONENTS OF QUALITY ASSURANCE
1. SOFTWARE TESTING
2. QUALITY CONTROL
3. SOFTWARE CONFIGURATION MANAGEMENT
5. SOFTWARE TESTING
• Software testing is an investigation conducted to provide stakeholders with
information about the quality of the product or service under test.
• Software testing can also provide an objective, independent view of
the software to allow the business to appreciate and understand the risks
of software implementation.
• Software testing is a popular risk management strategy. It is used to verify
that functional requirements were met.
7. QUALITY CONTROL
• Quality control (QC) is a procedure or set of procedures intended to ensure
that a manufactured product or performed service adheres to a defined set
of quality criteria or meets the requirements of the client or customer.
• Quality control is defined as the processes and methods used to monitor
work and observe whether requirements are met. It focuses on reviews
and removal of defects before shipment of products.
8. SOFTWARE CONFIGURATION MANAGEMENT
• Software Configuration Management (SCM) is the task of tracking and
controlling changes in the software, part of the larger cross-
disciplinary field of configuration management.
• It is concerned with the labeling, tracking and controlling changes in
the software elements of a system.
9. ELEMENTS OF SOFTWARE
CONFIGURATION MANAGAEMENT
SOFTWARE
CONFIGURATION
MANAGEMENT
Component
Identification
Version
Control
Configuration
Building
Change
Control