Validation Documentation: Common Pitfalls, Best Practices, and the Role of AI
Strengthen your documentation process through practical strategies, digital solutions, and strategic AI integration
December 17, 2025
11:00AM – 12:15 PM EST
Join us for an insightful webcast exploring the intricacies of validation documentation within the pharmaceutical and biotech industries. This session will examine common pitfalls that often lead to project delays and compliance challenges, while offering practical strategies to strengthen your documentation lifecycle. Learn how organizations are leveraging digital tools and AI-enabled solutions to enhance accuracy, streamline reviews, and maintain regulatory readiness.
What You’ll Gain:
- Identification of frequent documentation errors—and how to prevent the
- Strategies for aligning documentation practices with current regulatory expectations
- Insights into efficient document review, approval, and archival workflows
- Techniques for incorporating risk-based thinking into documentation processes
- Understanding how documentation quality affects timelines, audit outcomes, and compliance
- Best practices for training and engaging teams to uphold documentation standards
Who Should Attend:
- Validation and Quality Assurance professionals
- Regulatory Affairs specialists
- Project Managers overseeing validation activities
- Process engineers
- Compliance Officers
- Technical Writers and Documentation Specialists
- Anyone involved in the preparation, review, or approval of validation documentation
