Скачать или смотреть How Design Shapes Cleaning and Validation: Key Elements in GMP Manufacturing

Effective cleaning processes in pharmaceutical manufacturing begin with thoughtful design.
This video explains how design decisions such as equipment layout, cleaning location, automation level, materials of construction, and cleaning agent selection, create the foundation for consistent, well-controlled cleaning operations. These elements together determine how reliably a process can perform and how confidently its performance can be verified through cleaning validation.

You’ll learn how design influences:
• The way cleaning is carried out
• How much control and monitoring can be achieved
• The stability and reproducibility of operating conditions
• The type of evidence required during validation
• The overall reliability of cleaning performance in GMP environments

This video is ideal for professionals involved in:
Cleaning Validation • GMP Manufacturing • Quality Assurance • Quality Control • Engineering • Equipment Design • Process Development • Pharma Training and Compliance

Topics covered: cleaning process design, validation alignment, automation levels, materials and surface finish, contamination risk, cleaning agents, and the design–validation relationship across regulated environments.

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