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The Foundation Level course is aimed at anyone involved in software testing, such as testers, test analysts, test engineers, test consultants, test managers, user acceptance testers and software developers. This Foundation Level course is also appropriate for anyone who wants a basic understanding of software testing, such as project managers, quality managers, software development managers, business analysts, and IT directors.
If you are in a FDA regulated industry, NOPMARK Consulting strongly recommends you also register for the optional Medical Device Software Testing in a Nutshell below. This 1-day course is offered in conjunction with the 3-day ISTQB Foundation Level course at a discounted price.
The one-day Medical Device extension course is critical for all software testers working in the Medical Device and Healthcare industries. Learn the crucial elements of IEC 62304, ISO 14971, 21 CFR § 820.30, FDA General Principles of Software Validation, IEC 62366-1, and other applicable international and regulatory standards as they apply to software testing activities and deliverables.
Gain extra recognition for yourself with ASTQB Proficiency Distinction™. The new ASTQB Proficiency Distinction™ program is designed to extend the value of your standard ISTQB and ASTQB certifications by recognizing the value of intensive hands-on interactive training as part of the certification experience.
Have you passed the exam offered by ASTQB but have not taken an accredited Proficiency Distinction™ course? Qualify and achieve your Proficiency Distinction badge by taking this ASTQB-accredited Proficiency Distinction 1-Day Bootcamp course.
Agile testing is a current best practice approach to software testing that follows the principles of agile software development as outlined in the Agile Manifesto. A tester on an Agile project works differently than a non-Agile project. Testers must understand the values and principles that underpin Agile development process. The Agile Extension will give the tester the knowledge to be part of agile testing teams and achieve high performance.
If you are in a FDA regulated industry, NOPMARK Consulting strongly recommends you also register for the optional Medical Device Software Testing in a Nutshell course above. This 1-day course is offered in conjunction with the 2-day ISTQB Agile Tester course at a discounted price.
A 3-day course covering the multi-disciplinary nature of the user experience design process, design thinking, and the steps you can take to succeed. Learn how to apply user-centered design and UX throughout the design process to make medical technology safe, effective, usable, and satisfying for clinicians and patients.
Ambiguous, missing, or incomplete requirements? Requirements lacking good characteristics? Poorly derived and unstable requirements? Learn the skills to efficiently use requirements analysis to prepare valuable, estimable, and testable software requirements and user stories.
Software application testing is inefficient and ineffective if the tester is not well prepared to test it. The success of testing in a project is centered on how the Test Cases are designed and written for the various complex scenarios present in the project. This workshop also includes interactive exercises covering topics from requirements review, test case development, test case review, regression testing, and dozens of software testing tips & tricks.
Learn the why, when, where, and what to test using a live software application!
The three-day course covers the international and regulatory standards as they apply to software verification & validation with practical templates and hand-on exercises. You will utilize a real medical device in projects that will teach you how to create a software V&V plan, test procedure, and software V&V summary report that documents software verification & validation activities and complies with regulatory requirements.
This course is appropriate for software testers and test managers looking to build expertise in efficient compliance to all standards and regulations, while achieving high effectiveness in software testing.
Medical Device Risk Management
Learn the concepts of product and software risk management. Learn how to efficiently and effectively comply with ISO 14971, IEC 62304, and IEC 62366-1. This Risk Management course is aimed at R&D Engineers, Quality Engineers, project managers and product development team members involved in bringing medical devices to market.
Medical Device Design Verification & Validation
Design Verification and Validation are required as part of 21 CFR § 820.30. Learn how to effectively and efficiency plan and execute Verification and Validation activities throughout the product life cycle. This Design V&V course is aimed at R&D Engineers, Quality Engineers, Regulatory Analysts, and project managers The course also benefits engineering teams managing recent FDA 483 observations.