ValGenesis Process Manager: The Future of Cleaning Validation

Explore the future of cleaning validation with advancements in digitization and technology, and learn how to overcome traditional challenges while meeting increasingly stringent regulatory expectations with a science- and risk-based approach.

The current pharma and biopharma business environment requires operational flexibility in introducing new products, equipment, and technologies, and the impact on cleaning validation (CV) must be assessed in an agile and time-sensitive manner. However, in recent years, the number of cleaning- and cross-contamination-related observations issued by agencies such as the FDA has increased, indicating that regulatory expectations for effective and robust cleaning strategies are becoming more stringent.

In this webinar, we will present our expectations for the future of CV with advancements in cleaning technology and digitization, and how traditional methods are becoming obsolete in the context of the current business environment. Digitization will help overcome the challenges posed by paper-based processes that hinder optimization of asset usage and "right-first-time" CV, while mitigating regulatory risks through a science- and risk-based CV strategy using a digital and online life cycle management approach.

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