Kendi başına Medikal Cihaz olan ve bir medikal cihaza gömülü olarak çalışan yazılımların geliştirilmesinde baz alınan EN 62304 Tıbbi Cihaz Yazılım Yaşam Çevrimi standardı, Yazılımların belgelendirmesinde bulunması gereken teknik dosya gereklilikleri, Temel seviye yazılım test teknikleri EN 62304 standardının diğer standartlarla ilişkisi anlatılmıştır.
ISO-13485-2016.pptxPradeepa JThis document summarizes ISO 13485:2016, which outlines requirements for quality management systems for organizations involved in the design, development, manufacturing, installation, or servicing of medical devices. It contains 8 clauses that address the scope, documentation requirements, management responsibilities, and other criteria for quality management processes. Organizations that meet the ISO 13485 standard can receive certification to demonstrate their commitment to quality in the medical device industry.
IEC 62304: SDLC Conformance and Management MethodSense, Inc.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
Understanding IEC 62304MethodSense, Inc.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.
BASICS FOR ISO 9001 QMS LEAD AUDITOR COURSENithin V. JosephThe document discusses the basics of ISO 9001 quality management systems. It describes the Plan-Do-Check-Act (PDCA) cycle, also known as the Deming cycle or Shewhart cycle. PDCA involves planning improvements, implementing them, checking results, and acting to make further adjustments. The document also discusses the relationship between quality management and customer satisfaction, defining key terms like quality management systems, processes, ISO 9000, and ISO 9001. It explains that ISO 9001 defines requirements for a quality management system to meet customer and regulatory requirements.
Software as a Medical Device (SaMD) Challenges and Opportunities for 2021 and...Greenlight GuruThe SARS-CoV-2 pandemic drastically changes the landscape of digital health innovation. The FDA authorized emergency use for a variety of SaMD products including but not limited to mental health, clinical decision support and remote monitoring software applications. In addition, FDA recently launched the Digital Health Center of Excellence, provided updates on the pre-certification program, and host a session to convey FDA’s current thinking on AI/ML SaMD validation.
SaMD manufacturers must keep up with the fast-evolving regulatory landscape and optimize their software development practices with a goal to demonstrate conformance to the QMS requirements effectively and efficiently.
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
Understanding the New ISO 13485:2016 RevisionGreenlight Guruhe much anticipated revision to ISO 13485, the global medical device quality management system (QMS) standard, was released late last month (Feb, 2016).
The new ISO 13485:2016 ushers in a whole new wave of changes and requirements medical device manufacturers must adhere to, which we covered on our previous webinar here (http://www.greenlight.guru/webinar/iso-13485-2016-changes).
ISO tells us that there will be a three year transition period after which the guidance says, “any existing certification issued to ISO 13485:2003 will not be valid.”
The time to start planning your organization's transition to ISO 13485:2016 is now. Or face playing expensive catch up later.
(You can view the full webinar here: http://www.greenlight.guru/webinar/iso-13485-2016-transition-planning)
In this webinar, you'll learn specifically:
What your organization needs to be doing to prepare for the transition to ISO 13485:2016
Why the transition presents an opportunity for your organization to implement better processes
An overview of the specific changes coming with ISO 13485:2016
The actions you should be taking now and how to plan for the implementation of the standard
Iso 13485:2016Suhas RThis presentation consist of what ISO 13485 is and why is it important to consider this standard while designing a medical device. It will help u understand what Quality actual is and its importance in medical device industry. It gives you insight about quality management system and its documentation.
ISO 13485:2016 Revisions WebinarDQS Inc.The document summarizes changes between the 2003 and 2016 versions of ISO 13485, which provides requirements for quality management systems for organizations involved in the design and manufacture of medical devices. Some key changes include new requirements for risk management, supplier controls, feedback and verification/validation. The 2016 version also clarifies concepts, adds new definitions, and includes additional documentation requirements for areas like design and development and purchasing processes.
Iso13485 pptRajashekhara Gowda Medical devices – Quality management
systems – Requirements for regulatory
Purposes. ISO is an organization that develops Standards for use
worldwide.
ISO 13485 helps companies do their share in protecting
consumers and users of medical devices.
ISO 13485 Outlines criteria for a good Quality
Management System (QMS).
QMS criteria are good business practices ...
for example:
• Set Quality goals
• Ensure that regulations and other requirements are
understood and met
• Train employees
• Control your production processes
• Purchase from suppliers that can provide products that
meet your requirements
• Correct problems and make sure they do not happen again
Equipment qualification of medical deviceNahri MusyrifThe document defines key terms related to qualification and validation such as qualification, validation, commissioning, and calibration. It discusses classifying systems based on their impact on product quality and determining appropriate qualification approaches. Risk assessments are an important part of qualification and should be conducted according to GMP guidelines. Design, installation, operational, and performance qualifications are described as the key qualification steps. The importance of maintaining qualification status over the lifecycle is also covered.
Presentation: Conformity Assessment EvidenceTGA AustraliaAn introduction to conformity assessment procedures for medical devices, good manufacturing practice (GMP), some of the problems commonly experienced by sponsors and TGA, and helpful hints.
Test planNadia NaharThis document presents a test plan for version 1.0 of the IIT official website. It outlines the test items, features to be tested, approach, environment, responsibilities, and schedule. The test items include the website and its modules like achievements, gallery, news, programs, batches, courses, faculty, exams, results, groups, profile, documents, attendance, projects, calendar, and alumni. Features to be tested include adding, modifying, and viewing albums in the gallery module. The test plan follows IEEE 829 standards and will test the website on different client platforms.
Software Quality AssuranceRohana K AmarakoonThe document discusses topics related to software quality assurance and testing. It covers definitions of testing, types of testing activities like static and dynamic testing, different levels of testing from unit to system level. It also discusses test criteria, coverage, and agile testing approaches. The overall document provides an overview of key concepts in software quality assurance and testing.
INTEGRATED MANAGEMENT SYSTEM IMSSEHAR AREEJThis ppt will provide a complete overview of integrated management system in Pakistan.
in every sector like health, armed forces, business etc IMS is completely explained along all the ISO.
Design and development of medical deviceMalesh MThe document outlines the key steps in the medical device design and development process as required by ISO 13485. This includes establishing procedures for design and development stages, planning with target dates and reviews, determining inputs, producing outputs like drawings and bills of materials, conducting reviews and verification to ensure outputs meet inputs, performing validation to ensure the product meets requirements, and controlling any changes to the design.
Presentation: Medical Devices Single Audit Program (MDSAP) Pilot ProgramTGA AustraliaThis presentation provides an update on the progress of the Pilot and explores how the results of audits will be used by the participating Regulatory Authorities in support of market authorisation within their jurisdictions.
ASME BPVC 2021 Section IX - Qualification Standard for Welding, Brazing, and ...joshy38This document provides the qualifications and requirements for welding, brazing, and fusing procedures, welders, brazers, and welding, brazing, and fusing operators according to the ASME Boiler and Pressure Vessel Code. It defines the scope, types of tests, test positions, and variables that are required to qualify welding procedures and welding personnel. It also provides standards for documenting welding data, procedures, and qualifications.
DATA INTEGRITY GMP COMPLIANCEPharmaceuticalTrends changed from Non compliance to RR --> Gap to RR --> Data Integrity --> DIB --> Smart Audit & Smart Data.
RR = Regulatory Requirements
DIB = Data Integrity Breach
Take a serious Note for Data Integrity whether you are small or big organization. Your Data is the Heart of your business. Regulatory bodies are highly conscious about such issues. For beginners in this path, my small note can help you a lot.
ISO 13485: Quality Management System for Medical DeviceMananShah147368information about iso standard 13485 and its latest version and certification process
medical devices standards
IEC 62304 Action List MethodSense, Inc.IEC 62304 is an international standard that defines software development lifecycle requirements for medical device software. It requires that all aspects of the software development life cycle be scrutinized to ensure patient safety when software is involved. The standard establishes software safety classes A, B, and C based on the possible risk to health from software failures. It also outlines numerous requirements for each class, including developing plans, requirements, designs, testing procedures, problem resolution processes, and more. Upon completion, all documentation should be submitted to a test lab for review to obtain certification.
Computer System ValidationGMP EDUCATION : Not for Profit OrganizationThis presentation describes approaches for software validation used to automate laboratory research procedures, consolidate data collection and analysis and/or run sophisticated QC or manufacturing operations.
Several approaches to software validation exist and may be appropriate for a specific project.
The scope of any validation effort depends upon a number of factors
Size and complexity of the software,
Origin of the software (custom vs. off-the-shelf) and
Whether the functions are critical or non-critical in nature.
By effectively planning the process, validation time and resources can be reduced while meeting regulatory requirements.
ISO 13485: What's Next?Greenlight GuruWhile ISO 13485 is written in black and white, the alignment between the standard's requirements and expectations is not always clear - especially in regards to SaMD (software as a medical device). This session will discuss aligning ISO 13485 with best practices for SaMD, and how we can expect the shift of the industry to impact the anchor standard of the medical device industry.
This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.
Splunking HL7 Healthcare Data for Business ValueSplunkHealthcare data is time-oriented and diverse. HL7 (Health Level Seven International) is a set of interoperability standards, formats and definitions for exchanging data between software applications used by healthcare providers. In this session, learn how to leverage HL7 data for business value. Through a presentation and demo’s, we will discuss a variety of HL7 use cases from exploring HL7 data within Splunk, addressing missing orders investigations, queuing up integrations, and others. Also, you can learn about the health of the system that is providing these services by using Splunk ITSI.
Difference between fda 21 cfr part 820 and ISO 13485Anil ChaudhariThe document compares FDA 21 CFR Part 820 and ISO 13485 quality management standards. ISO 13485 is an international voluntary standard that specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and services that consistently meet regulatory requirements. In contrast, FDA 21 CFR Part 820 outlines current good manufacturing practice regulations in the US that govern the design, manufacture, and distribution of medical devices to ensure safety and effectiveness. Key differences include ISO 13485 being a global voluntary standard while FDA 21 CFR Part 820 is mandatory for medical device manufacturers selling products in the US.
Quality Assurance in SDLCAdil Mughal- The document discusses quality assurance in the software development lifecycle, including key concepts, practices, and challenges.
- It defines quality assurance, software development lifecycle phases, and differences between verification and validation. Common testing types like unit, integration, and non-functional testing are also covered.
- The document then describes quality assurance practices used in industry, such as creating QA plans, requirements reviews, test case development, and validation activities at different stages. Finally, challenges of quality assurance are discussed around testing focus, cost of fixes, schedules, and career opportunities.
Medical Device Regulation (MDR) overview for Technion, May 25, 2021Levi ShapiroOn May 26, 2021, the EU introduced the most sweeping changes to the Medical Device legal framework since the mid 90's. Ulf Grundmann, Senior Partner, King & Spalding (Frankfurt), reviews some of these regulatory changes, from the perspective of medical device innovators. The presentation includes Scope and Definitions, Classification and Conformity Assessment, Placing a Device on the EU Market, UDI and EUDAMED, Supply Chain Obligations, PMS and Vigilance
Yazılım Mimarileri - Yazılım Geliştirme ModelleriKubra KoseYazılım Mimarileri
Yazılım Geliştirme Modelleri
Hızlı Uygulama Geliştirme Modeli
Denetimli Adımlar Modeli ( RUP)
ISO 13485:2016 Revisions WebinarDQS Inc.The document summarizes changes between the 2003 and 2016 versions of ISO 13485, which provides requirements for quality management systems for organizations involved in the design and manufacture of medical devices. Some key changes include new requirements for risk management, supplier controls, feedback and verification/validation. The 2016 version also clarifies concepts, adds new definitions, and includes additional documentation requirements for areas like design and development and purchasing processes.
Iso13485 pptRajashekhara Gowda Medical devices – Quality management
systems – Requirements for regulatory
Purposes. ISO is an organization that develops Standards for use
worldwide.
ISO 13485 helps companies do their share in protecting
consumers and users of medical devices.
ISO 13485 Outlines criteria for a good Quality
Management System (QMS).
QMS criteria are good business practices ...
for example:
• Set Quality goals
• Ensure that regulations and other requirements are
understood and met
• Train employees
• Control your production processes
• Purchase from suppliers that can provide products that
meet your requirements
• Correct problems and make sure they do not happen again
Equipment qualification of medical deviceNahri MusyrifThe document defines key terms related to qualification and validation such as qualification, validation, commissioning, and calibration. It discusses classifying systems based on their impact on product quality and determining appropriate qualification approaches. Risk assessments are an important part of qualification and should be conducted according to GMP guidelines. Design, installation, operational, and performance qualifications are described as the key qualification steps. The importance of maintaining qualification status over the lifecycle is also covered.
Presentation: Conformity Assessment EvidenceTGA AustraliaAn introduction to conformity assessment procedures for medical devices, good manufacturing practice (GMP), some of the problems commonly experienced by sponsors and TGA, and helpful hints.
Test planNadia NaharThis document presents a test plan for version 1.0 of the IIT official website. It outlines the test items, features to be tested, approach, environment, responsibilities, and schedule. The test items include the website and its modules like achievements, gallery, news, programs, batches, courses, faculty, exams, results, groups, profile, documents, attendance, projects, calendar, and alumni. Features to be tested include adding, modifying, and viewing albums in the gallery module. The test plan follows IEEE 829 standards and will test the website on different client platforms.
Software Quality AssuranceRohana K AmarakoonThe document discusses topics related to software quality assurance and testing. It covers definitions of testing, types of testing activities like static and dynamic testing, different levels of testing from unit to system level. It also discusses test criteria, coverage, and agile testing approaches. The overall document provides an overview of key concepts in software quality assurance and testing.
INTEGRATED MANAGEMENT SYSTEM IMSSEHAR AREEJThis ppt will provide a complete overview of integrated management system in Pakistan.
in every sector like health, armed forces, business etc IMS is completely explained along all the ISO.
Design and development of medical deviceMalesh MThe document outlines the key steps in the medical device design and development process as required by ISO 13485. This includes establishing procedures for design and development stages, planning with target dates and reviews, determining inputs, producing outputs like drawings and bills of materials, conducting reviews and verification to ensure outputs meet inputs, performing validation to ensure the product meets requirements, and controlling any changes to the design.
Presentation: Medical Devices Single Audit Program (MDSAP) Pilot ProgramTGA AustraliaThis presentation provides an update on the progress of the Pilot and explores how the results of audits will be used by the participating Regulatory Authorities in support of market authorisation within their jurisdictions.
ASME BPVC 2021 Section IX - Qualification Standard for Welding, Brazing, and ...joshy38This document provides the qualifications and requirements for welding, brazing, and fusing procedures, welders, brazers, and welding, brazing, and fusing operators according to the ASME Boiler and Pressure Vessel Code. It defines the scope, types of tests, test positions, and variables that are required to qualify welding procedures and welding personnel. It also provides standards for documenting welding data, procedures, and qualifications.
DATA INTEGRITY GMP COMPLIANCEPharmaceuticalTrends changed from Non compliance to RR --> Gap to RR --> Data Integrity --> DIB --> Smart Audit & Smart Data.
RR = Regulatory Requirements
DIB = Data Integrity Breach
Take a serious Note for Data Integrity whether you are small or big organization. Your Data is the Heart of your business. Regulatory bodies are highly conscious about such issues. For beginners in this path, my small note can help you a lot.
ISO 13485: Quality Management System for Medical DeviceMananShah147368information about iso standard 13485 and its latest version and certification process
medical devices standards
IEC 62304 Action List MethodSense, Inc.IEC 62304 is an international standard that defines software development lifecycle requirements for medical device software. It requires that all aspects of the software development life cycle be scrutinized to ensure patient safety when software is involved. The standard establishes software safety classes A, B, and C based on the possible risk to health from software failures. It also outlines numerous requirements for each class, including developing plans, requirements, designs, testing procedures, problem resolution processes, and more. Upon completion, all documentation should be submitted to a test lab for review to obtain certification.
Computer System ValidationGMP EDUCATION : Not for Profit OrganizationThis presentation describes approaches for software validation used to automate laboratory research procedures, consolidate data collection and analysis and/or run sophisticated QC or manufacturing operations.
Several approaches to software validation exist and may be appropriate for a specific project.
The scope of any validation effort depends upon a number of factors
Size and complexity of the software,
Origin of the software (custom vs. off-the-shelf) and
Whether the functions are critical or non-critical in nature.
By effectively planning the process, validation time and resources can be reduced while meeting regulatory requirements.
ISO 13485: What's Next?Greenlight GuruWhile ISO 13485 is written in black and white, the alignment between the standard's requirements and expectations is not always clear - especially in regards to SaMD (software as a medical device). This session will discuss aligning ISO 13485 with best practices for SaMD, and how we can expect the shift of the industry to impact the anchor standard of the medical device industry.
This presentation originally aired during the 2022 Future of QMS Requirements Virtual Summit.
Splunking HL7 Healthcare Data for Business ValueSplunkHealthcare data is time-oriented and diverse. HL7 (Health Level Seven International) is a set of interoperability standards, formats and definitions for exchanging data between software applications used by healthcare providers. In this session, learn how to leverage HL7 data for business value. Through a presentation and demo’s, we will discuss a variety of HL7 use cases from exploring HL7 data within Splunk, addressing missing orders investigations, queuing up integrations, and others. Also, you can learn about the health of the system that is providing these services by using Splunk ITSI.
Difference between fda 21 cfr part 820 and ISO 13485Anil ChaudhariThe document compares FDA 21 CFR Part 820 and ISO 13485 quality management standards. ISO 13485 is an international voluntary standard that specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and services that consistently meet regulatory requirements. In contrast, FDA 21 CFR Part 820 outlines current good manufacturing practice regulations in the US that govern the design, manufacture, and distribution of medical devices to ensure safety and effectiveness. Key differences include ISO 13485 being a global voluntary standard while FDA 21 CFR Part 820 is mandatory for medical device manufacturers selling products in the US.
Quality Assurance in SDLCAdil Mughal- The document discusses quality assurance in the software development lifecycle, including key concepts, practices, and challenges.
- It defines quality assurance, software development lifecycle phases, and differences between verification and validation. Common testing types like unit, integration, and non-functional testing are also covered.
- The document then describes quality assurance practices used in industry, such as creating QA plans, requirements reviews, test case development, and validation activities at different stages. Finally, challenges of quality assurance are discussed around testing focus, cost of fixes, schedules, and career opportunities.
Medical Device Regulation (MDR) overview for Technion, May 25, 2021Levi ShapiroOn May 26, 2021, the EU introduced the most sweeping changes to the Medical Device legal framework since the mid 90's. Ulf Grundmann, Senior Partner, King & Spalding (Frankfurt), reviews some of these regulatory changes, from the perspective of medical device innovators. The presentation includes Scope and Definitions, Classification and Conformity Assessment, Placing a Device on the EU Market, UDI and EUDAMED, Supply Chain Obligations, PMS and Vigilance
Yazılım Mimarileri - Yazılım Geliştirme ModelleriKubra KoseYazılım Mimarileri
Yazılım Geliştirme Modelleri
Hızlı Uygulama Geliştirme Modeli
Denetimli Adımlar Modeli ( RUP)
Building the continuous integration layer in AveaOguzhan OzavarKaynak Kod Yönetimi, Build & Deployment Otomasyonu, Test Odaklı Geliştirme, Statik Kod Analizi, Test Otomasyonu, Lab Yönetimi, Çevik İterasyonlar, Pipeline Yönetimi
Windows Small Business Server 2008 Yedekleme Yönetimi ve Disaster Recovery Su...sbs2008Windows Small Business Server 2008 Yedekleme Yönetimi ve Disaster Recovery yöntemlerini tüm detaylarıyla gösteren bir sunumdur.
Windows Small Business Server 2008 Yedekleme Yönetimi ve Disaster Recovery Su...Mustafa Windows Small Business Server 2008 Yedekleme Yönetimi ve Disaster Recovery yöntemlerini tüm detaylarıyla gösteren bir sunumdur.
Bir CMMI Seviye 5 Organizasyonel Performans Yönetim Projesi Örneği: Kod Kalit...Deniz GungorBu sunum UYMS (Ulusal Yazılım Mühendisliği Sempozyumu) 2017 Antalya’da sunulan `Bir CMMI Seviye 5 Organizasyonel Performans Yönetim Projesi Örneği: Kod Kalitesini İyileştirmek ` başlıklı makalenin sunumudur.
Makaleye ulaşmak için aşağıdaki linke tıklayınız.
http://ceur-ws.org/Vol-1980/UYMS17_paper_86.pdf
This presentation is a presentation of the article titled "A CMMI Level 5 Organizational Performance Management Project Example: Improving Code Quality" presented at the UYMS (National Software Engineering Symposium) 2017 Antalya.
Click on the link below to access the article or published paper.
BTRisk Yazılım Güvenliği Yönetimi EğitimiBTRisk Bilgi Güvenliği ve BT Yönetişim HizmetleriYazılım Güvenliği Yönetimi Eğitimimiz aşağıdaki konu başlıklarını içermektedir:
Güvenli Yazılım Geliştirme Modelleri
-TOUCHPOINTS
-Secure Development Lifecycle (Microsoft)
-CLASP (Comprehensive, Lightweight Application Security Process)
Risk Yönetimi
Güvenlik Gereksinim Analizi
Teknik Riskler
Sızma Testi ve Statik Kod Analizi
Güvenlik Operasyonu
Odoo ile MRP, PLM, Kalite ve Bakım YönetimiMehmet DemirelOdoo ile MRP, PLM, Kalite ve Bakım Yönetimi. MRP Programı, Malzeme ihtiyaç planlaması, MRP Yazılımı, Üretim kaynak planlaması, ERP Programı, Kurumsal Kaynak Planlama Yazılımı
Çevik Yaklaşım, Scrum ve XPOsman DÖNER, PMP, PMI-ACPÇevik(Agile) değer ve prensipleri, geleneksel yaklaşımdan farklarını ele alan, Scrum Çerçevesi ile XP(Extreme Programming) pratiklerinin anlatıldığı detaylı bir sunum.
2. Kapsam ve Genel Bilgiler
• Tasarım + Bakım
• Validasyon Kapsam Dışıdır.
• Kendi başına satılan ve Gömülü Yazılımlar
• EN 14971
• EN 13485
• Temel Test Prensipleri
• Medikal CE Teknik Dosya Gereklilikleri
4. Giriş, Genel Gereklilikler ve Sınıflandırma
• Sınıf A, Sınıf B ve Sınıf C
• Sınıf C + Donanım Önlemi = Sınıf B
• Sınıf B + Donanım Önlemi = Sınıf A
• Risk olasılığı %100 Risk tahmini dayanağı şiddete göre
• Süreçler, Aktiviteler, Görevler
5. Planlama
Üretici yazılımın bütün süreçlerini içeren bir planlama
yapmalı bu planlamayı güncel tutmalı ve yazılı hale
getirmelidir. Planlama yazılım geliştirme modelini
içermelidir.
• Planlama her bir aşamada kullanılacak süreçleri,
aktiviteleri ve görevleri açıklamalıdır.
• Planlamada izlenebilirlik
• Konfigürasyon ve değişiklik yönetimi
• Problem ve hata giderme yönetimi
6. Planlama
• Sistem gereklilikleri
• Standartlar, metotlar ve araçlar
• Entegrasyon ve test
• Doğrulama
• Risk Yönetimi
• Dokümantasyon
• Konfigürasyon
• Destekleyici araçlar
• Konfigürasyon araçları (doğrulamadan önce)
7. Yazılım Gereklilikler Analizi
• Gerekliliklerin tanımlanması
• Gerekliliklere risk kontrol önlemlerinin eklenmesi
• Yazılım gereklilikleri belirlendikten sonra tıbbi cihaz risk
analizinin tekrar değerlendirilmesi
• Yazılım gerekliliklerinin güncel tutulması
• Yazılım gerekliliklerinin doğrulanması
8. Yazılım Mimari Tasarımı
• Sistem gerekliliklerinin mimari tasarıma dönüştürülmesi
• Yazılım parçalarının etkileşiminin tasarlanması
• SOUP performansı ve fonksiyonelliği
• SOUP donanım ve yazılım gerekliliği
• Risk kontrolüne tabi yazılım parçalarını ayırma
• Mimari tasarımın doğrulanması
9. Yazılım Detaylı Tasarımı
• Mimarinin Yazılım Parçalarına dönüştürülmesi
• Arabirimlerin detaylı tasarımı
• Detaylı tasarımın doğrulanması
10. Yazılım Parçalarının Devreye Sokulması ve
Doğrulaması
• Yazılım parçalarının devreye sokulması
• Yazılım parçaları doğrulama sisteminin kurulması
• Yazılım parçalarının kabul kriterlerinin belirlenmesi
• Yazılım parçalarının doğrulanması
11. Yazılım Entegrasyonu ve Entegrasyon Testi
• Yazılım parçalarının entegrasyonu
• Entegrasyonun doğrulanması
• Entegre edilmiş yazılımın test gerekliliklerinin
belirlenmesi ve test gerekliliklerinin doğrulanması
• Regresyon testlerinin gerçekleştirilmesi
• Test sonuçlarının içeriği
• Hata giderme sisteminin kullanılması
12. Yazılım Sistem Testi
• Yazılım gereklilikleri için testlerin kurulması ve
gerçekleştirilmesi
• Hata giderme sürecinin işletilmesi
• Değişikliklerden sonra tekrar test
• Sistem testlerinin doğrulanması
• Sistem test kayıtlarının oluşturulması
13. Yazılımın Serbest Bırakılması
• Yazılım doğrulamanın tamamlanması
• Bilinen kalan anormalliklerin yazılı hale getirilmesi
• Bilinen kalan anormalliklerin değerlendirilmesi
• Serbest bırakılan versiyonun dokümante edilmesi
• Serbest bırakılan yazılımın nasıl üretildiğinin dokümante
edilmesi
• Yazılımın arşivlenmesi
• Serbest bırakılmanın tekrar edilebilir olduğundan emin
olunması
14. Yazılımın Bakımı
• Yazılımın bakım planının oluşturulması
• Geri beslemenin izlenmesi ve değerlendirilmesi
• Hata giderme süreçlerinin izlenmesi
• Değişiklik isteklerinin analizi ve onayı
• Kullanıcı ve otoriteler ile iletişim
• Modifikasyonların yürürlüğe sokulması
• Değiştirilmiş yazılımın serbest bırakılması
15. Yazılımın Risk Yönetimi -1
• Yazılımda riskin meydana gelme olasılığı %100dür.
• Tehlikeli durum oluşturabilecek yazılım parçalarının tespiti
• Tehlikeli durum oluşturabilecek potansiyel nedenlerin
tespiti
• Yayınlanan SOUP anormallik listesinin analizi
• Potansiyel sebeplerin yazılı hale getirilmesi
• Tehlikeli durum oluşturabilecek olayların sırasının yazılı
hale getirilmesi
• Risk kontrol önlemlerinin tanımlanması, bu önlemlerin
yerine getirilmesi, doğrulanması
• Yeni risk yaratabilecek olaylar sırasının tanımlanması
16. Yazılımın Risk Yönetimi -2
• Risk dokümantasyonunun izlenebilirliği
• Değişikliklerde risk yönetimi
17. Yazılımın Konfigürasyon Yönetimi
• Konfigürasyon parçalarının tanımlanması
• SOUPların tanımlanması
• Sistem konfigürasyon dokümantasyonunun tanımlanması
• Konfigürasyon değişikliği onayı, gerçekleştirilmesi ve
doğrulanması
• Değişikliğin izlenebilmesi
• Konfigürasyon durumunun izlenmesi
18. Yazılımın Problem Çözümü Süreci
• Problem raporlarının alınması
• Problemin araştırılması
• Problem hakkında ilgili kişilere bildirim yapılması
• Kayıtların tutulması
• Problem çözümünün doğrulanması
• Yazılımın test edilmesi
19. Yazılım Teknik Dosyasında Olması Gerekenler
• Risk Yönetim Dosyası
• Yazılım güvenlik sınıflandırması
• Yazılım tasarım planı
• Yazılım sistem gereklilikleri
• Yazılım Mimari tasarımı
• Yazılım test planı
• İzlenebilirlik tablosu
• Yazılım test raporu
• Kalan anormallikler
• Konfigürasyon yönetimi dosyası
21. 7 Test Prensibi
• Testin amacı yazılımda hataların olduğunu göstermektir,
yazılımda hata kalmadığını göstermek değildir.
• Yazılımı %100 test etmek imkansızdır
• Teste yazılım geliştirme sürecinin başında başlanmalıdır.
• Hatalar yazılımın belli alanlarında yoğunlaşır
• Böcek ilacı paradoksu; sürekli aynı yerleri test edersek
hata bulamayız, test senaryolarını güncellemek gereklidir.
• Test yaklaşımı ve aktiviteleri yazılım projesinin koşullarına
göre değişir.
• Yeni hata bulamıyoruz başarılı bir yazılım ürettik demek
yanılgıdır. Hatasız yazılım müşteri ihtiyaçlarını tam
karşılıyor anlamına gelmez.