Tool Qualification Kit for NI TestStand Test Management Software



Similar documents
DO-254 Requirements Traceability

Meeting DO-178B Software Verification Guidelines with Coverity Integrity Center

NI Global Services. Innovate With Confidence Reduce Development Time Minimize Long-Term Maintenance Costs. ni.com/services

WIND RIVER RTCA DO-178 SOFTWARE CERTIFICATION SERVICES

October 21 November 5 November 14 December 12. Washington DC Boston Chicago San Jose. ni.com

Best practices for developing DO-178 compliant software using Model-Based Design

ALL PRODUCTS MFG & SUPPLY

DO-178B compliance: turn an overhead expense into a competitive advantage

Intland s Medical Template

INTRODUCTION. This book offers a systematic, ten-step approach, from the decision to validate to

Essentials of the Quality Assurance Practice Principles of Testing Test Documentation Techniques. Target Audience: Prerequisites:

IBM Rational systems and software solutions for the medical device industry

Life Sciences Product Development Artifacts Survey Results

Implementing Title 21 CFR Part 11 (Electronic Records ; Electronic Signatures) in Manufacturing Presented by: Steve Malyszko, P.E.

Camar Aircraft Products Co. QUALITY MANUAL Revision D

Efficient Verification for Avionic Product Development

Certification Authorities Software Team (CAST) Position Paper CAST-9

How To Write Software

Anwendung von Polyspace im Software Entwicklungsprozess nach IEC München, , Dr.-Ing. Jörg Barrho

QUALITY MANAGEMENT SYSTEM MANUAL

Considerations When Validating Your Analyst Software Per GAMP 5

AC REUSABLE SOFTWARE COMPONENTS

Camber Quality Assurance (QA) Approach

MDEP Generic Common Position No DICWG 02

IBM Rational Rhapsody

Software Engineering for LabVIEW Applications

Using TechExcel s DevSuite to Achieve FDA Software Validation Compliance For Medical Software Device Development

SAFE SOFTWARE FOR SPACE APPLICATIONS: BUILDING ON THE DO-178 EXPERIENCE. Cheryl A. Dorsey Digital Flight / Solutions cadorsey@df-solutions.

From Chaos to Clarity: Embedding Security into the SDLC

The Impact of RTCA DO-178C on Software Development

CHARTER. Interagency Information Systems Working Group. Timber Regulation and Forest Restoration Program June 23, 2015

Quality Management System Manual

Certification of a Scade 6 compiler

System Build 2 Test Plan

codebeamer INTLAND SOFTWARE codebeamer Medical ALM Solution is built for IEC62304 compliance and provides a wealth of medical development knowledge

Qualtech Consulting Inc.

MHRA GMP Data Integrity Definitions and Guidance for Industry March 2015

The SaaS LMS and Total Cost of Ownership in FDA-Regulated Companies

NI 6601/6602. Contents CALIBRATION PROCEDURE. ni.com/manuals

Overview Presented by: Boyd L. Summers

Supporting FISMA and NIST SP with Secure Managed File Transfer

Quality Assurance System Manual

Configuration Management Practices

Decodability QUALITY. A New Method to Ensure Bar Code Quality throughout the Distribution Channel

21 CFR Part 11 White Paper

Reduce Medical Device Compliance Costs with Best Practices.

ISO 9001:2008 Audit Checklist

"Creating an automated test station to verify AdBlue pump modules in hydraulic test." - Jiří Kubíček, Robert Bosch, spol. s r.o.

Versity All rights reserved.

Software Development Tools for Safety-Critical, Real-Time Systems Handbook

and Certification What Does It Take To Get Certified? Steven Hoenig NJ Business Unit Manager

Software Development for Medical Devices

FSW QA Testing Levels Definitions

DO-178B/C Differences Tool

PRAGMA ENGINEERING Srl. Next-Generation ATS (Sistemi ATE di Nuova Generazione)

Understanding DO-254 Compliance for the Verification of Airborne Digital Hardware

Dependable (Safe/Reliable) Systems. ARO Reliability Workshop Software Intensive Systems

Certification Authorities Software Team (CAST) Position Paper CAST-26

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE

HHS OCIO Policy for Information Technology (IT) Enterprise Performance Life Cycle (EPLC)

The Software Development Life Cycle (SDLC)

Welcome! Frank Teleso. Quality Manager

Thermo Scientific icap 7000 Series ICP-OES. Low cost ICP-OES analysis high quality data

asuresign Aero (NATEP Grant MA005)

ENEA: THE PROVEN LEADER IN SAFETY CRITICAL AVIONICS SYSTEMS

AP1000 European 18. Human Factors Engineering Design Control Document

Computer System Configuration Management and Change Control

SECTION 4 TESTING & QUALITY CONTROL

Improving Embedded Software Test Effectiveness in Automotive Applications

UL Qualified Firestop Contractor Program Management System Elements. March 13, 2013

Oracle Insurance Policy Administration System Quality Assurance Testing Methodology. An Oracle White Paper August 2008

Project Management Guidelines

Table of Contents 1. SCOPE APPLICABLE DOCUMENTS TERMS AND DEFINITIONS QUALITY MANAGEMENT SYSTEM...4-8

(COMPANY LOGO) CGMP COMPUTERIZED SYSTEM VENDOR AUDIT QUESTIONNAIRE

AEROSPACE STANDARD. Quality Management Systems - Requirements for Aviation, Space and Defense Organizations RATIONALE

SOFTWARE QUALITY & SYSTEMS ENGINEERING PROGRAM. Quality Assurance Checklist

AS 9100 Rev C Quality Management System Manual. B&A Engineering Systems, Inc Business Park Drive, Suite A-1 Costa Mesa, CA 92626

Reaping the benefits of Reusable Software Components

How to Leverage Your QMS for Competitive Advantage. Katie Farrand Continuous Improvement Specialist Synergy Resources

Interactive Guidance for Safety Critical Avionics

DRAFT REGULATORY GUIDE

Software Test Plan (STP) Template

Effective Software Verification for Medical Devices

Description of Services for A Quality Assurance Engineer for SQA Assignment for eservices Development Projects ICTA/CON/IC/P5/411B

8. Master Test Plan (MTP)

FDA Software Validation-Answers to the Top Five Software Validation Questions

DeltaV SIS for Burner Management Systems

MHRA Data Integrity Guidance and Expectations Document

The Impact of 21 CFR Part 11 on Product Development

The Comprehensive and Fully Compliant Certification Solution. Certification Services

AEROSPACE QUALITY MANAGEMENT SYSTEM

Implementation of ANSI/AAMI/IEC Medical Device Software Lifecycle Processes.

Computer System Configuration Management and Change Control

BPA Policy Cyber Security Program

Cartel Electronics. AS 9100 Quality Systems Manual

ISOLATING UNTRUSTED SOFTWARE ON SECURE SYSTEMS HYPERVISOR CASE STUDY

New Program Quality Requirements for Suppliers (NPQR) For Limited Manufacturing of Components and/or Processes for Engineering Certification

Transcription:

www.certtech.com Tool Qualification Kit for NI TestStand Test Management Software CertTech, L.L.C. 14425 College Blvd. Suite 140 Lenexa, KS 66215 P (913-814-9770) F (913-817-0837)

CertTech s TestStand Qualification Kit provides a solid foundation for achieving formal qualification of the National Instrument s TestStand Tool used for automated product verification and validation testing in rigorous regulatory environments. Overview Verification and Validation (V&V) are critical process elements of the product life cycles used in safety or mission critical software, hardware and system development. This is particularly important in regulated industries, such as medical devices, pharmaceuticals, rail transportation, aerospace and military applications, which must adhere to rigorous process guidelines to achieve approval by regulatory agencies and certification authorities. Effective use of test automation can save significant time and effort in complex development projects, and is encouraged by regulatory authorities as a means of reducing human error that is inherent in the process. Qualification of the test automation tools allows for the tool outputs to be trusted as true and correct, and eliminates the need for costly and time consuming manual review and analysis of the test tool outputs. Test automation can maximize the speed, efficiency and flexibility of testing and its use is encouraged by regulatory authorities to reduce errors. The Challenge The use of tools to eliminate, reduce or automate processes in the product development lifecycle is common in many companies across multiple industries. Tools are typically categorized for either development or verification activities and appropriate qualification processes are defined for each. Development tools produce outputs that become part of the product itself, and therefore can introduce errors or defects in the product design. Verification tools do not produce outputs that become part of the product, and therefore cannot introduce defects or errors in the product design. They may, however, fail to detect defects or errors. Here is the real challenge; in accordance with DO-178B/C and other regulatory guidelines, verification tools such as NI s TestStand must be qualified if any required regulatory processes are eliminated, reduced or automated. Qualification of development tools typically requires the same level of process rigor applied to the product development artifacts. Qualification of verification tools generally involves creation of a qualification plan, definition of operational requirements, verification of the requirements, and maintaining the tool artifacts in a suitable configuration management system. Verification tools such as TestStand must be qualified if any regulatory processes are eliminated, reduced or automated. 1

The Solution CertTech LLC has created a qualification kit for NI s TestStand. We have extensive experience in regulated industries and functional safety standards and thoroughly understand the requirements for using qualified tools specified by standards like DO- 178C and ISO 26262. The TestStand Tool Qualification Kit can significantly reduce the time and cost of formal tool qualification by: Supporting tool qualification processes for DO-178C, ISO 26262 and other regulations. Providing a comprehensive set of requirements and test coverage for common TestStand features. Delivering an extensive suite of tests verifying the provided requirements. Offering a readily extendable framework that allows for coverage extension as needed. Providing often required TQP, TOR, TQAS, test trace matrix and review documentation. The TestStand Tool Qualification Kit significantly reduces the time and cost of formal tool qualification. The Tool Qualification Kit also produces the documentation that will be needed as the necessary artifacts for compliance. This documentation is essential because the overall goal is to show complete transparency for the verification process so the test can be recreated and every detail is clear on what was done. The Kit provides tremendous value to companies across a wide variety of safety and mission critical industries, where rigorous product development processes demand the highest levels of assurance. With some of the newer functional safety standards like ISO 26262 and DO-178C, there is specific information requiring the projects to use qualified tools for verification and validation activities that will not be manually reviewed, which inherently places additional emphasis on using qualified tools like NI TestStand---and the TestStand Tool Qualification Kit. Below is a listing of the Tool s contents; Generic Tool Qualification Plan (TQP) Generic Tool Operational Requirements (TOR) - Station configuration, report options, data types - Sequence file properties, sequences, variables, parameters - LabVIEW, LabWindows CVI and C/C++ Adapters - Expressions operators and functions - Step properties, steps using adapters, sequence calls, flow control, statements, labels, message pop-ups and waits Requirements-based Verification Procedures Generic Tool Qualification Accomplishment Summary (TQAS) document Test Trace Matrix providing correlation of requirements with specific tests Sequence for running the qualification tests and generating pass/fail results Individual sequences for testing the features of TestStand 2

Cost Analysis The examples below detail the average internal costs involved in tool qualification by project size, compared to use of the TestStand Tool Qualification Kit. Expense line items will vary. Project Size Small Medium Large Larger Average Product Life Expectancy 30 yrs 30 yrs 30 yrs 30 yrs Average Revision Cycle 5 yrs 5 yrs 5 yrs 5 yrs Revision Cycles Through Product Life 6 6 6 6 Average Code Size (KSLOC)* 25 75 150 300 Average Test Results Review Time 2 2 2 2 In Hours Per 1 KSLOC Burdened Labor Rate Per Hour ** $75 $75 $75 $75 Expense of Review Time $22,500 67,500 $135,000 $270,000 (#KSLOC x 2hrs x Rate x Cycles) Cost of the Tool Qualification Kit*** $24,999 $24,999 $24,999 $24,999 Cost Savings ($2,499) $42,501 $110,001 $245,001 Footnotes * KSLOC; 1000 Source Lines of Code ** Estimated fully burdened labor rate for experienced software engineer, DO-178C, Level A; $150,000 USD per year, $75/hr. *** Further pricing information available upon contact. **** Savings do not reflect ongoing revision service costs. DER Compliance Statement* The TestStand tool is used to automate the collection and analysis of test data during requirementsbased verification testing activities and complies with all applicable process and documentation requirements for Verification Tools as defined in section 12.2 of RTCA/DO-178B and FAA Order 8110.49 Chapter 9, as well as Section 12.2 of RTCA/DO-178C and RTCA/DO-330. The tool qualification artifacts including the Tool Qualification Plan (TQP), the Tool Operational Requirements (TOR), the Test Procedures and Verification Results (TPVR), the raw test result files (actual and expected), and this Tool Qualification Accomplishment Summary (TQAS) have been archived in accordance with the applicable configuration management processes and procedures, and are available for review. * Summary of Compliances/Findings/Observations Report for CertTechTestStand Tool Qualification Kit. July 27 th, 2012; Mr. Thomas C. Roth, FAA, Designated Engineering Representative (DER). 3

Significantly Reduce the Time and Cost of Formal Tool Qualification An Experienced Partner CertTech has extensive experience providing high quality V&V services in a variety of regulatory environments, including formal qualification of software development and verification tools used to increase efficiency of the product development and certification processes. CertTech s team of engineering professionals provides innovative products, systems and services in support of the development of advanced technology products, focusing primarily on the development of automated test solutions. 14425 College Blvd., Suite 140 Lenexa, KS 66215 913-814-9770 www.certtech.com National Instruments, NI and ni.com are trademarks of National Instruments. CertTech, CertTech, LLC and certtech.com are trademarks of CertTech, LLC. Other product and company names listed are trademarks or trade names of their respective companies. 4