Prepare for a successful global study by allocating additional time to strategize localization and translation.
Back to team page
Patrick McCormack
Director
Patrick has 10 years of experience applying HFE/UE to the development of medical devices with an emphasis on ensuring safe and effective use as part of the FDA approval process. He possesses expertise in the interpretation and implementation of various design standards, including IEC 62366, AAMI HE75, BS EN ISO 14971, and others. Patrick has a BS in Human Factors Psychology from Embry-Riddle Aeronautical University.



Bold facts
Learn more about

What is your favorite way to give back to the community?

What fictional universe would you like to live in?

In your spare time (or if you had spare time), you would absolutely do this:

Your favorite city in the world is...and why?

You cannot start the day without doing this:

Your ultimate celebrity dinner party guest list would include:

Long-term personal or professional goal?

Any other facts to share?
Read our team’s latest bold insights
How to prepare products for global research
Understanding and accounting for common challenges is the first step in collecting high quality data during global research.
Support a company culture of self-advocacy with these four tips
Uncover insights to encourage a self-advocacy culture with authentic employee engagement.
Improve medical device safety with these packaging design tips
Safe and effective medical device use starts with designing packaging that considers the unique needs of its users.