Integrating Git version control with validation systems automates medical device software traceability, ensuring instant ...

Averna's Matt Thompson shares strategies to avoid common traps when transitioning medical devices from R&D to manufacturing.

Shashank Murali is a Quality Assurance professional based in Minneapolis, Minnesota, with more than eight years of experience in the medical device technology area.

Drug & Device Team provides recommendations based on Food & Drug Administration (FDA) draft guidance on Quality Management System ...

A DevOps-based framework integrates automation, continuous integration, and agile methodologies to enhance medical device software development.

Joint effort centers on design validation, pre-compliance, and OTA/interoperability testing; Advantech AIW-173 modules target ...

The Global Electronic Design Automation (EDA) Market was estimated to be worth USD 541 Million in 2023 and is forecast to a ...

On track to submit GraftAssureDx™ for FDA review by year-endOn track for commitment to have 20 transplant centers globally ...

The approach enables DFT and design verification (DV) teams to operate in parallel, accelerating development cycles while improving fault coverage. This cohesive strategy not only boosts test ...

Continues Execution of Strategic Transformation and Advancement of Biologics Pipeline FREMONT, CA / ACCESS Newswire / November 14, 2025 / Tivic Health® Systems, Inc. , a diversified immunotherapeutics ...

Certification enhances global market readiness, reinforces quality systems, and supports Zomedica's long-term growth strategy ANN ARBOR, MI / ACCESS Newswire / November 6, 2025 / Zomedica Corp. (" ...

Continues Execution of Strategic Transformation and Advancement of Biologics Pipeline FREMONT, CA / ACCESS Newswire / November 14, 2025 / Tivic Health® Systems, Inc. (Nasdaq:TIVC), a diversified immun ...