ANNOUNCEMENTS AND SPOTLIGHTS

Connect Human Factors to Every Stage of Development
From early user research and formative testing to labeling, validation, and production readiness, human factors help keep the user at the center of device development. Our integrated PDE teams bring that perspective into the decisions that shape product success.

Use the Evidence You’re Already Generating More Strategically
Integrated evidence planning helps align studies, endpoints, and decisions already in motion so evidence can support regulatory, payer, clinical, and commercial needs.

August 26 - 27

Boston, MA

September 28 - October 1

Barcelona, Spain

Veranex Client Atraverse Makes Successful Strategic Exit

We surfaced a workflow gap nobody had spec'd for. Three years later, J&J acquired the system.

The Medical Device Workshop Readiness Checklist

A failed workshop doesn't just waste a day. It derails entire programs. Run this checklist first.

Closing the Imaging Gap in Preclinical Neurosurgery

MRI goes dark once the craniotomy starts. Intraoperative ultrasound catches brain shift while surgeons can still correct it.

Legacy Medical Devices: Refresh Insights for Your Next Generation

What got your Gen 1 device to market won't get you through Gen 2. Three regulatory shifts catching teams off guard, and where the budget should move instead.

What the Proposed EU MDR Revision Means for You

The EU's proposed MDR/IVDR overhaul touches certification timelines, clinical evidence, and innovation pathways. Catch up if you missed it.

How to Avoid FDA Warning Letters

Warning letters are public, permanent, and preventable. Catch up on the prevention and response guide if you missed it.