How can you measure the effectiveness of your GMP documentation improvements?
Good Manufacturing Practice (GMP) documentation is essential for ensuring quality, compliance, and safety in the production of pharmaceuticals, biologics, medical devices, and other regulated products. However, documentation can also become a source of inefficiency, confusion, and errors if it is not updated, organized, and aligned with the current processes and standards. That is why GMP documentation improvement is a key aspect of quality management and continuous improvement. But how can you measure the effectiveness of your GMP documentation improvement efforts? Here are some tips and tools to help you.