Interface Analysis Associates

07/27/2026

Calling all current adult Ozempic® pen users in the San Jose area!

We're looking for adults who currently self-administer Ozempic® to participate in a usability research study taking place in late August.

✅ Sessions take less than 30 minutes. Pays $200 Cash.

Interested? Click the link in the comments to complete a brief Google interest survey.

07/23/2026

We are looking for 8 adults in the Bay Area who have been diagnosed with a medical condition and are currently taking medication to participate in a one-time, 45-minute usability study evaluating a new medication delivery device.

If you have participated in a study with us within the past 6 months, you may not be eligible.

Please note: Not everyone who expresses interest or contacts us will qualify or be selected to participate. Eligibility is determined during the screening process, and participant selection is based on the study's requirements.

If you're interested, we'd love to hear from you! Please contact us at 408-907-6866 to see if you qualify.

07/23/2026

07/22/2026

We are looking for 10 registered nurses for a study located in Saratoga, CA taking place in August 2026.

Give us a call at (408) 907-6866 to do a short phone screening.

Due to limited study availability and eligibility requirements, not everyone who contacts us will qualify or be selected to participate.

07/22/2026

How detailed should a URRA be? When does a task become critical? And how closely should a URRA align with other risk management documents?

These are some of the most common questions human factors and regulatory teams face when developing Use-Related Risk Analyses (URRAs) for medical devices and combination products.

In IAA's latest white paper, "Demystifying the Use-Related Risk Analysis (URRA)," you'll learn:
✔ The purpose and role of the URRA
✔ Common misconceptions and FDA feedback
✔ Critical task identification and validation planning
✔ Practical strategies for developing a robust URRA

Download the white paper and companion FAQ: https://interfaceanalysis.com/insights/demystifying-the-use-related-risk-analysis/

Learn the purpose of the URRA, common misconceptions, FDA expectations, and practical strategies for human factors validation programs.

07/21/2026

Thank you to everyone who joined us for last week's webcast on "Creating an FDA‑Ready Moderator's Script for Your Human Factors Validation Study."

We appreciated the thoughtful discussion and questions around moderator script development, study ex*****on, and considerations for supporting successful human factors validation studies.

This session is part of an ongoing webcast series in partnership with the Regulatory Affairs Professionals Society (RAPS). Our next webcast is planned for October 7—be sure to stay tuned for more details.

07/14/2026

We are looking for First Responders in the San Jose, CA area to participate in several short, paid rescue simulation sessions.

Please share this information with anyone who may be interested, or give us a call if you would like 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

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

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.

07/04/2026

From all of us at IAA, we wish you a safe and happy Fourth of July.