• ON-DEMAND WEBINARS

    Cost-Effective Compliance Through a Risk-Based Approach to Validation  

    The FDA defines validation as “establishing documented evidence that provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes.” What does that mean for your company? How do you determine

    the required compliance level? How do you implement a practical and scalable approach to validation that is accepted and encouraged by FDA? Hear industry expert Patrick Lennon and share in the answers to these questions during this free on-demand webcast. 



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