Useful Information

2026.01.15

Understanding GxP Data: A Comprehensive Guide for Pharmaceutical Quality and Compliance

2026.01.15

From “Validation” to “Verification”: The Evolution of CSV Approaches

2026.01.15

Why Human Errors Occur

2026.01.15

Proper Methods for Correcting Source Data

2026.01.15

The Boiled Frog Phenomenon and the AI Generation

2026.01.15

Data Integrity and Human Error

2026.01.15

FDA Inspection Process: From Implementation to Completion

2026.01.15

FDA Guidance Revision for Computer Systems Used in Clinical Investigations

2026.01.15

The Origins of GMP (Good Manufacturing Practice)

2026.01.15

The Historical Development of GMP Regulations and FDA Inspection Systems: Continuous Evolution in Protecting Patient Safety