Nov

2016

FDA New 510(k) MRI Device Submission Guidance

FDA issued a revised and final guidance: “Submission of Premarket Notifications for Magnetic Resonance Diagnostic Devices” November 18, 2016 to replace the 1988 guidance.
Section 4.2.2 requests a description of how cardiac and peripheral nerve stimulation control is implemented including discussion of software mechanisms to limit gradient output and how the operator is notified if peripheral nerve stimulation is possible.

Section 4.2.8 Image Processing indicates that the software is generally considered Moderate Level of Concern and refers to the general, OTSS, and cybersecurity FDA software guidances. This section also requests detailed information for each image processign feature telated to algoirthms, inputs and data formats, level of user interactio, outputs and how they are displayed.

Section 9.2.7 requests a summary of post processign features and the the software version.

PrevNext

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

FDA New 510(k) MRI Device Submission Guidance

SoftwareCPR Training Courses:

Subscription Services

Corporate Office