Ranorex Automated Test Tool

Ranorex Automated Test Tool

Our test team at SoftwareCPR® often uses Ranorex Automated Test Tool for automated integration level and software system level testing.   We have had very good experience with this tools for user interface testing for certain types of medical device software.  The test reports are particularly impressive and well suited for Design History Files (DHF).

Accelerate testing for desktop, web and mobile applications

Ranorex Automated Test Tool empowers testers with a complete toolset for end-to-end testing of desktop, web and mobile applications in a single license. Automate tests on a Windows desktop, and then execute them locally or remotely, on real iOS or Android mobile devices or on simulators/emulators. Run tests in parallel and accelerate cross-browser testing for Chrome, Firefox, Safari, Microsoft Edge, and more. With Ranorex Automated Test Tool, you and your team will spend less time resolving issues with unstable tests and more time assessing the quality of your application.

Powerful reporting features

Monitor the results of testing with an overview of the test execution flow, including pie charts, screenshots, and detailed error logs that are easily readable for testers, developers, and project managers alike.  View a comprehensive test report within Ranorex Automated Test Tool, save it as a PDF or automatically receive it as an email attachment. Customize the report to fit your needs. Generate jUnit-compatible reports for easy integration with CI tools.  Reduce debugging time by jumping to a failed test step directly from a test report, or use the maintenance mode to repair tests on the fly while the test is still running.

If you have questions about the pros and cons of this tool, or if you want our test team to help jump-start your team or even outsource creation of test assets for use with this tool, let us know by leaving a message below or email Paul Felten directly at pfelten@softwarecpr.com.  You can view Paul’s credentials and the credentials for all of our partners on our Team page!

SoftwareCPR Training Courses:

Being Agile & Yet Compliant (Public)

Our SoftwareCPR unique approach to incorporating agile and lean engineering to your medical device software process training course is now open for registration!

  • Agile principles that align well with medical
  • Backlog management
  • Agile risk management
  • Incremental and iterative software development lifecycle management
  •  Frequent release management
  • And more!

3 days virtual (Zoom) with group exercises, quizzes, examples, Q&A.

Lead Instructor: Mike Russell

Next public offerings:

  • Americas: 11-13 February 2025
  • EU/Eastern Europe/Middle East/Africa/Atlantic/eastern South America: 18-20 February 2025
  • Southern Central Northeastern Pacific: 24-26 February 2025
Register using form at this link:     Agile Course Post Promo

 

IEC 62304 and other emerging standards for Medical Device and HealthIT Software

Our flagship course for preparing regulatory, quality, engineering, operations, and others for the activities and documentation expected for IEC 62304 conformance and for FDA expectations. The goal is to educate on the intent and purpose so that the participants are able to make informed decisions in the future.  Focus is not simply what the standard says, but what is meant and discuss examples and approaches one might implement to comply.  Special deep discount pricing available to FDA attendees and other regulators.

3-days onsite with group exercises, quizzes, examples, Q&A.

Instructor: Brian Pate

Next public offering:  TBD

Call or email now to schedule a private, in-house class. The fall schedule is filling up!

Email training@softwarecpr.com to request a special pre-registration discount.  Limited number of pre-registration coupons.

Registration Link:

TBD

 


 

Medical Device Cybersecurity (Public or Private)

This course takes a deep dive into the US FDA expectations for cybersecurity activities in the product development process with central focus on the cybersecurity risk analysis process. Overall approach will be tied to relevant standards and FDA guidance documentation. The course will follow the ISO 14971:2019 framework for overall structure but utilize IEC 62304, IEC 81001-5-1, and AAMI TIR57 for specific details regarding cybersecurity planning, risk characterization, threat modeling, and control strategies.

2-days onsite with group exercises, quizzes, examples, Q&A.

Instructor: Dr Peter Rech, 2nd instructor (optional)

Next public offering:  TBD

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