Interface Analysis Associates

Interface Analysis Associates

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IAA has over 30 years of experience conducting non-clinical, paid usability studies. All of our studies are non-invasive, fun and you get paid to participate!

07/14/2026

Tomorrow is the day.

Join us for a free webcast, in partnership with Regulatory Affairs Professionals Society (RAPS), on "Creating an FDA‑Ready Moderator's Script for Your Human Factors Validation Study."

We'll discuss practical considerations, common challenges, and key elements to consider when preparing for a human factors validation study.

Earn 1.0 RAC credit
July 15 | 12–1 PM ET

Register here: https://www.raps.org/learn-develop/events/sponsored-webcast-creating-an-fda-ready-moderator-s-script-for-your-human-factors-validation-study.html

Sponsored Webcast: Creating an FDA-Ready Moderator’s Script for your Human Factors Validation Study 07/08/2026

A moderator's script is more than a study guide; it helps ensure consistency across participants and contributes to the overall success of a human factors validation study.

When developed thoughtfully, a moderator's script can help teams gather insights while supporting FDA expectations for study ex*****on.

Join us next Wednesday, July 15, as we discuss practical considerations for creating an FDA‑ready moderator's script for your human factors validation study.

▶️ Earn 1.0 RAC credit
▶️ July 15 | 12–1 PM ET

Register here: https://www.raps.org/learn-develop/events/sponsored-webcast-creating-an-fda-ready-moderator-s-script-for-your-human-factors-validation-study.html

Sponsored Webcast: Creating an FDA-Ready Moderator’s Script for your Human Factors Validation Study A moderator’s script is central to human factors validation. It operationalizes the protocol, ensures consistent ex*****on, data collection, and FDA compliance. This webcast shares a proven approach refined through FDA reviews.

Sponsored Webcast: Creating an FDA-Ready Moderator’s Script for your Human Factors Validation Study 06/25/2026

Developing a moderator's script for your human factors validation study?

Join us for a free webcast, presented in partnership with Regulatory Affairs Professionals Society (RAPS), exploring key considerations for creating an FDA‑ready moderator's script that supports effective study ex*****on and defensible results.

✅ FDA‑aligned best practices
✅ Insights from experienced human factors professionals
✅1.0 RAC credit
✅ July 15 | 12–1 PM ET

Save your spot: https://www.raps.org/learn-develop/events/sponsored-webcast-creating-an-fda-ready-moderator-s-script-for-your-human-factors-validation-study.html

Sponsored Webcast: Creating an FDA-Ready Moderator’s Script for your Human Factors Validation Study A moderator’s script is central to human factors validation. It operationalizes the protocol, ensures consistent ex*****on, data collection, and FDA compliance. This webcast shares a proven approach refined through FDA reviews.

06/19/2026

Today, we recognize Juneteenth.

Juneteenth marks the end of slavery in the United States—June 19, 1865, when federal troops arrived in Galveston, Texas, and announced that enslaved people were free.

It’s a moment to reflect on this history and the ongoing work to build systems and environments that are equitable for all.

We encourage our team, partners, and community to take time today to learn and reflect.

06/11/2026

Study for Radiologists located in the United States.

I work for Dr. Anthony Andre and Interface Analysis Associates. We are a usability study firm located in Saratoga, CA.

We are evaluating a new software program that takes imagery from an ultrasound scan (e.g, GE system) and then aids the radiologist by using AI-assisted imaging analysis along with other tools that allow better, more rapid, and more quantifiable detection of abnormalities. The goal is to enable the radiologist to view, analyze and report faster, and with greater accuracy.

The proposed software would integrate with your EHR system and allow you to open and view raw ultrasound files with an enhanced suite of AI-assisted visualization and analysis tools.

The makers of the software are outside of the US and have utilized radiology subject matter experts in the development of the software and now seek to evaluate it with US-based radiologists.

Your participation will provide valuable feedback towards optimizing the user experience and to ready the product for validation and FDA submission.

Time commitment is 30 - 60 minutes

Compensation is $550

Can be done remotely with proper set up but do need some to come in locally.

Thank you for your time!

Jeana Nishihara
Office Manager
Dr. Anthony Andre
Interface Analysis Associates
408-834-8443 (desk)
[email protected]

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Telephone

Address


1821 Saratoga Avenue
Saratoga, CA
95070

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm