08

Apr

2015

HumanFactorsCPR Consulting Services

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Crisis Prevention and Recovery, LLC (CPR) is excited to announce the formation of a new business speciality, HumanFactorsCPR. HumanFactorsCPR is the fourth business speciality under the CPR brand, joining SoftwareCPR, ValidationCPR, and RegulatoryCPR.
“One of the most attractive features of our new HumanFactorsCPR services is our capability to bridge the risk analysis process with the usability engineering process and expert human factors-based design and testing”, states Alan Kusinitz. “We have always been known for our unique expertise with risk management, but nowwith addition of a human factors expert, we can carry the process forward for our clients with planning and management of formative and summative studies to evaluate the effectiveness of the risk controls.”

HumanFactorsCPR can help medical device and HealthIT companies plan an effective usability engineering program to comply with IEC 62366 and FDA guidance for human factors content in regulatory submissions. For more information,email brian@HumanFactorsCPR.com.

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 offering: Dec 3, 4, & 5, 2024 – 12:00 pm to 5:00 pm CET

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