Arianna Krenk - Performance Validation

Arianna has supported cGMP compliance projects for the pharmaceutical and medical device industry since 2018. Her area of focus is qualification of new product development for med device. Her experience includes documentation creation, review, approval, and routing, electronic document database management, and qualification of new medical device product.

Brad Henry

Vice President of Services Products - Brad has over 20 years of experience managing and executing CQV projects for the pharmaceutical and medical device industries. He has extensive experience in dry products, parenteral, facilities and utilities, and in-vitro diagnostics.

Schedule with Brad Henry