Validation Documentation: Avoiding Common Mistakes That Lead to Delays
September 17, 2025
11:00AM – 12:15 PM EST

Join us for an insightful webcast focusing on the intricacies of validation documentation within the pharmaceutical and biotech industries. This session will delve into common pitfalls that often lead to project delays, offering practical strategies to ensure your documentation processes are robust, compliant, and efficient. Gain firsthand knowledge from industry experts on maintaining high-quality validation records that withstand regulatory scrutiny.

What You’ll Gain:

• Identification of frequent documentation errors and how to prevent them
• Strategies for aligning documentation practices with current regulatory expectations
• Insights into effective document review and approval workflows
• Techniques for integrating risk-based approaches into validation documentation
• Understanding the impact of documentation quality on project timelines and compliance
• Best practices for training teams on documentation standards and procedures

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