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The Transition from New Product Development to Process Validation: Key Components for an Optimal Validation Outcome (Individual)

This presentation will provide an overview of the key factors to consider for the development of a robust process validation, ensuring that a process that is being implemented can produce allografts that is processed consistently while meeting predetermined specifications.

Grace Bolton, MS, SLBB

CEO and Founder

QVEX Consulting, LLC

Grace Bolton has more than 20 years of combined experience in the tissue banking and medical device industry. Her expertise includes, but is not limited to, equipment qualification, test method validation, quality assurance, process validation, cleanroom certification, environmental monitoring, sterilization, and regulatory compliance. She is a dynamic and innovative professional well versed in creating Master Validation Plans for various aspects of validation.

She is the CEO and Founder for QVEX Consulting, LLC. Her consulting firm focuses on validation needs assessments, mitigating risk and implementing validation systems that meets FDA requirements and other regulatory compliance, following applicable standards and guidance documents such as AATB, USP and AAMI/ISO.

Grace is also currently serving as a Medical Device and Sterilization SME for Tunnell Government Services, Inc., where she works directly with the FDA to perform extensive review for FDA submissions and as a sterility consultant for various types of submissions.

Before forming QVEX Consulting. LLC, she worked at LifeLink Tissue Bank, as the Director of Validation, where she developed and managed a robust environmental and validation program and spearheaded several Master Validation Plans, which includes equipment qualification, method suitability testing, packaging validation, transport container validation, and shelf-life validation.

She has also served as a task force member for 2 of AATB’s guidance documents, Microbiological Process Validation & Surveillance Program and Qualification of Packaging Validation and Validation of Shipping/Transport Procedures.

Grace holds a BS degree in Microbiology and a MS degree in Quality Assurance, along with a Graduate Six Sigma Black Belt Certification.

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The Transition from New Product Development to Process Validation: Key Components for an Optimal Validation Outcome
Select the "View On-Demand Recording" button to begin.  |  60 minutes
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