Regulatory expectations in the pharmaceutical and biotechnology industries continue to evolve. Recent updates from the United States Pharmacopeia (USP), combined […]
The FDA has updated cleanroom validation requirements for pharmaceutical manufacturers. Learn about the key changes, implementation timelines, and how to
Emerging technologies are revolutionizing cleanroom design and validation. Explore how AI-powered monitoring systems, advanced filtration technologies, and automated validation processes
Equipment validation failures can delay production and risk compliance. Discover the five most common mistakes pharmaceutical companies make during equipment
