REDWOOD CITY, Calif.--(BUSINESS WIRE)--Box, Inc. (NYSE:BOX), the leading Content Cloud, today announced that its native e-signature product, Box Sign, has achieved support for compliance with FDA 21 ...

FDA finds widespread quality issues at three Philips medical device facilities, citing violations in manufacturing and complaint handling.

The webinar highlights opportunities in enhancing system validation, utilizing agile and waterfall methodologies, and leveraging COTS, SaaS, IaaS, PaaS, and cloud solutions to meet FDA requirements ...

The main market opportunities lie in providing solutions for secure digital record management and compliance with FDA regulations. Companies can capitalize on the demand for effective Quality ...

The "21 CFR Part 11 Compliance for SaaS/Cloud Application (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering. Join the "21 CFR Part 11 Compliance for SaaS/Cloud ...

The market opportunities lie in leveraging data process mapping to enhance data integrity and regulatory compliance, particularly aligning with FDA standards. There's potential in addressing gaps, ...

Market opportunities arise from the growing need for modernization and compliance assurance in FDA-regulated industries focusing on data integrity. Emphasizing cloud computing, automation, and mobile ...

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course" training has been added to ResearchAndMarkets.com's offering. This ...

NEW YORK, NY / ACCESS Newswire / November 14, 2025 / For decades, plastics have moved through the world without an identity.

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

The "21 CFR Part 11 Compliance for SaaS/Cloud Application (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's offering.