What Do Regulators Check for When Auditing Cleaning & Cleaning Validation? | NSF International

Поделиться
HTML-код
  • Опубликовано: 12 сен 2024
  • In this webinar, David Waddington looks at the most common European and U.S. FDA regulatory findings related to basic cleaning issues including cross contamination and approaches to cleaning validation. He also highlights key changes in GMP guidance and discusses QP considerations such as the appropriate use of quality risk management and HBEL assessments.

Комментарии •