The pharmaceutical industry relies on robust cleaning processes and validation to ensure product quality and patient safety. ASTM International, a global standards organization, provides essential guidance that supports this critical area.
“Clean systems, cleaner outcomes—ASTM standards make it possible.”
ASTM standards, such as those for cleaning validation and contamination control, offer pharmaceutical organizations well-defined, scientifically grounded methodologies. These standards help streamline cleaning protocols, ensure regulatory compliance, and maintain consistent product quality. For instance, ASTM E3106 outlines best practices for cleaning validation, providing a risk-based framework to verify that cleaning processes effectively remove residues.
Adopting ASTM standards not only simplifies regulatory audits but also drives efficiency and innovation in cleaning techniques, enabling manufacturers to achieve higher reliability in their operations. With the support of ASTM standards, pharmaceutical companies can confidently meet stringent quality requirements while optimizing their processes.
Explore more about ASTM standards and their applications in pharmaceuticals at ASTM International.
Reserve your seat now for the 2nd Cleaning Process & Validation Conference in Prague!
