In pharmaceutical and biotech manufacturing, cleaning validation (CV) compliance gaps rarely stem from a lack of expertise. More often, they arise from the limitations of manual and hybrid processes — data gaps, inconsistent documentation, arbitrary assessments, and insufficient validation planning.  

This webinar explores how digital cleaning validation helps organizations move beyond document-driven, static workflows to system–driven, proactive validations. You’ll learn how digitalization reduces risk, strengthens data integrity, and improves audit readiness while enabling more efficient, consistent execution. 

Key topics include: 

• Root causes of compliance risks in traditional CV workflows 

• Hidden blind spots created by manual data transfer, interpretation, and review 

• How digital solutions enforce standardized templates, guided evidence capture, controlled approvals, and real-time program visibility   

• Benefits to data integrity (ALCOA+), traceability, and audit readiness 

• A practical demonstration of a digital CV workflow  

• Strategies for implementing digital solutions without disrupting operations, including change control, training, and system validation 

• Real-world outcomes, including faster reviews, fewer deviations, reduced findings, and stronger QA oversight