News

Many organizations manage the fundamentals—routine calibrations, label checks, and process logs—but achieving true compliance in life sciences requires going beyond ...

SQA Services is sponsoring the Generis American Medical Device Summit 2025 in Chicago. Join our Lunch & Learn Roundtable on ...

Prevent recurring issues in medical devices with RCCA—drive compliance, quality, and patient safety.

Highlights from the PDA Regulatory Conference: AI in compliance, predictive quality, training evolution, and FDA inspection readiness strategies.

Stay informed with SQA’s Q1 2025 Regulatory Surveillance Summary, featuring key updates from FDA, EMA, WHO, ANVISA, NMPA, and other ...

In the life sciences industry, packaging is far more than a box or a seal. It is a validated system—a ...

Bringing a new device to market is one of the most critical milestones for any manufacturer. It’s a driver of ...

Implementing PPAP effectively doesn’t just reduce regulatory risk—it can save time and money across the medical device industry supply chain.

In a recent episode of Bridge the Gap, hosted by Dale Zwizinski and Adam Jay from Revenue Reimagined, Michael Guymon, ...

Review key 2024 regulatory shifts still influencing 2025—covering pharma, medical devices, AI, cosmetics, and global compliance strategies.

SQA Regulatory Surveillance Summary for May and June 2024 By: Laurel Hacche, Rocio Cabeza, and Debra Cortner Agência Nacional de ...

SQA Regulatory Surveillance Summary for March and April 2024 By: Laurel Hacche, Rocio Cabeza, and Debra Cortner Brazil: Agência Nacional ...