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. 

    Start With a Phone Call

    Speak with one of our SME's. The result may be: 

    • Advice 
    • Free Consultation 
    • Gaining a trusted advisor and networking partner

    Our offerings are as flexible as our clients’ needs and range from staff augmentation to
    scalable turn-key solutions and we look forward to hearing from you.