The compliance process at pharmaceutical manufacturers is complicated because many still use paper-based systems to record manufacturing steps. These paper records are reviewed by FDA auditors to ...

This article explores the US and EU compliance requirements to ensure patient safety for GMP ancillary materials in cell and ...

Study the top-performing companies across all manufacturing industries and a plain and simple truth emerges: the ability to produce consistently high-quality products, regardless of the forces ...

Life science companies must adhere to the FDA’s Good Manufacturing Practices (GMP) in manufacturing and storage of the product within their manufacturing facility. For example, GMP compliance is ...

Regulating manufacturing processes in the medical device industry is challenging. But process signature verification can help manufacturers get a handle on problems before they get out of control.

CPHI Frankfurt 2025 will highlight advancements in pharmaceutical process control, patient safety, and efficiency, addressing automation, material performance, and regulatory compliance challenges.

Compliance should be more than a box to check. When done right, it can strengthen operations, protect product quality and keep workers safe. But 95% of manufacturing companies still use paper-based ...

The manufacturing process is a complex one that can be impacted by many factors: supplies, equipment, factory overhead, the need for special parts, and the people who work at all points in the process ...

If you want to optimize the use of machinery, materials and labor and ensure orders are completed on time and to standard, then a digital workflow is a great step towards creating a smarter ...