PMI Minnesota Chapter - Professional Development has partnered with agilityIRL to provide a discounted price for Agile Education & Scrum Certifications.
Agile Education, Certification and Coaching for Teams, Leaders and Organizations
Promo Code: PMI-CARS ($400 Discount)
To register for the upcoming class, click: https://www.tickettailor.com/events/agilityirl/882951?
WHAT IS CARS™?
Our exclusive Certified Agile Regulatory Specialist™ (CARS™) program is for those employing Agile in an FDA-regulated and QMS-governed environment. It has been designed and developed—and is presented—in collaboration with agilityIRL and Agile Quality Systems, pioneers in Agile development.
Like all agilityIRL products and services, CARS™ is agile-driven but reality-based. Its design and development flow from our decades of personal experience with Agile in medical device product development and participation on the team that authored AAMI TIR45: 2012. CARS™ has been created by a team that includes individuals that literally wrote the book on using Agile in medical device product development.
CARS™ is Agile-Driven But Reality Based
At agilityIRL, we have distinctive experience in the life science industry. With this experience, we understand the critical nuances of operating an Agile framework (e.g., Scrum, SAFe, etc.) in an environment regulated by the Food and Drug Administration (FDA) and governed by a company’s own Quality Management System (QMS). For those working to become agile in this industry, our CARS™ program is a great fit.
Our 2-Day Program
Our CARS™ program is a 2-day class that teaches you field-proven concepts, rules, methods and tools for incorporating Agile in an FDA regulated and QMS governed environment. Following the program, candidates with qualifying class attendance and participation, as determined by the instructor, will be eligible to take an exam to earn their CARS™ certification.
Training Instructors:
Kelly Weyrauch
A practical expert on Agile Software Development, Certified Scrum Master (CSM), and SAFe Program Consultant (SPC) who applies the theories, principles, and requirements from regulations, standards, and development models to the real-world context of regulated, safety-critical medical device software and systems.
Dates:
Mon Sep 11, 2023 9:00 AM - Tue Sep 12, 2023 5:00 PM CDT
Please contact Chair – Professional Development for questions related to registration [email protected]