Why Established Pharma Sites Need A Digital Cleaning Validation Strategy

By Saurabh Joshi, Senior Director of Industry Solutions, ValGenesis

As pharmaceutical manufacturers push the boundaries of innovation, a critical segment of the industry often struggles to keep pace: long-established, mature production facilities. These sites are the backbone of global medicine supply, which delivers essential treatments to millions of patients daily. Yet, many still rely on outdated systems and manual workflows—particularly in cleaning validation, a foundational process that directly affects product quality and patient safety. The core challenge lies in modernizing these legacy operations without disrupting production or risking regulatory compliance.

Fortunately, digital transformation is offering a path forward. Advanced digital tools are enabling these facilities to streamline cleaning validation, enhance traceability, and maintain audit readiness—all while improving operational efficiency. In today’s regulatory landscape, digitalization is no longer optional; it’s essential for ensuring consistent quality and staying competitive.

If you're managing or supporting a mature pharmaceutical site, now is the time to explore how digital solutions can revolutionize your cleaning validation processes.