Design Controls Module 4:
Risk Management

This module of the Design Control Series explores the requirements for risk management and implementation tools to meet the requirements in a 1.5-hour webinar. Take a deep dive into case studies that you can apply today to achieve easier FDA submissions and get the inside scoop directly from the FDA on how to understand your risks, improve your design and limit your liability. 
 

Expert Faculty

Pat Baird
Product Design Owner
Baxter Healthcare

Richard Chapman
Chief, General Hospital Devices Branch in the Office of Device Evaluation (ODE) of the Center for Devices and Radiological Health
FDA

(Expert faculty titles and companies may have changed since the time of recording.)
 

Level

Intermediate
 

Learning Impact

Upon completion of this training, participants will:

  • Gain working knowledge of Design Control requirements across the Total Product Lifecycle (TPLC)
  • Understand the interdependencies across functional responsibilities on successful product design and launch
  • Get an overview of key regulations and guidances
  • Obtain Design Controls Professional Certificate (if all 10 webinar courses are viewed and certificate exam passed)


Certification

Certificate of Completion: Each participant will receive a Certificate of Completion for .1 CEUs upon viewing the webinar course and returning a completed evaluation form.

Professional Certificate: Each participant who views all 10 webinar modules and successfully passes the final exam will receive a Professional Certificate (1.0 CEU) from Xavier University. The final exam can be taken remotely after the last module.
 

Price

$99 per module
$840 for entire series (Receive a 15% discount for purchasing all 10 modules)