Capture

Thursday, May 7, 2015
2:30PM – 6:30PM
2:00PM – 2:30PM Registration
2:30PM – 5:30PM Course (Lectures, Exercises, Discussions)
5:30PM – 6:30PM Dinner and Networking

Location:
University of Memphis
3rd Floor Fogelman College Classroom Building
Central Avenue at Innovation Drive

Cost: $225 Professional, $100 Student, +$75 after May 1st
Includes Dinner, Completion Certificate, and Parking

Great Solutions Start with Great Requirements
Great ones can make everything better
Bad ones can make everything worse

Improve your software and systems development by increasing quality, productivity, and documentation for traceablity.

Requirements are the foundation of any successful project. Clear expectations and traceability during the development process is of upmost importance, especially in highly regulated, safety-critical industries like medical devices. By writing high-quality requirements to begin with, we know that we are building the correct product that behaves in the desired fashion under increasingly complex scenarios, enabling complete traceability from conceptual prototyping to regulatory submission. The project benefits most when everyone on the development team understands and practices this systems-thinking approach.

Please join us for a tool-neutral course with a focus on requirements management (RM) during the medical device development process:

• Why is RM important in medical device development?
• What are some RM best practices that can be easily implemented?
• What does RM look like for everyone involved in medical device development (marketing, engineer, PM, medical practitioner)?

At the end of the course, you will receive a 90 day trial of BlueMix

Please Bring your Laptops

CLICK HERE TO REGISTER