ValGenesis Inc., the market leader in enterprise validation lifecycle management systems (VLMS), and Performance Validation, Inc. a 100% employee-owned company serving the life sciences industry since 1988, have partnered to deliver unique compliance-focused digital validation solutions for life sciences companies in the US. Performance Validation is an industry leader with over 30 years of experience […]
Performance Validation an industry leader with 35 years of experience in analyzing, identifying, and testing the most critical elements of the manufacturing process for FDA-regulated industries is proud to announce the appointment of Donna Griffith as the company’s Director of Technical Services. Donna Griffith brings a wealth of experience and expertise to Performance Validation, having […]
Computer System Validation (CSV) is crucial for any organization that needs to comply with Good Laboratory Practices (GLPs). GLPs are regulatory quality standards for conducting non-clinical laboratory studies that support the development of products for human or animal health. They require that laboratory data be reliable, consistent, and accurate. To meet these requirements, laboratories that […]
In today’s competitive job market, professionals aren’t just seeking a paycheck; they’re looking for a sense of belonging and an opportunity to be part of something bigger. At Performance Validation (PV), we understand this aspiration, which is why our Employee Stock Ownership Plan (ESOP) stands at the core of our culture and business philosophy. The […]
In the high-stakes world of pharmaceutical manufacturing, equipment maintenance isn’t just a routine part of the job—it’s a cornerstone of our success and reliability. As technology evolves and the complexity of our systems increases, the way we approach equipment diagnostics must also adapt. We’re not just maintaining machines; we’re ensuring the continuous, compliant output that […]
Performance Validation (PV) is pleased to welcome Scott Council as the new Division Director for PV’s North Carolina Hub. Scott’s extensive engineering background, combined with his experience in manufacturing and FDA-regulated environments, make him the perfect fit to lead PV’s operations in North Carolina. As a North Carolina native and North Carolina State University graduate, […]
For Immediate Release (Indianapolis, Indiana; June 16, 2014). Performance Validation is pleased to announce that Ms. Stephanie Welte has successfully completed certification as a Certified Quality Auditor. The Certified Quality Auditor is a professional who understands the standards and principles of auditing and the auditing techniques of examining, questioning, evaluating and reporting to determine a […]
Indianapolis, IN (August 2015) Performance Validation, a nationwide leader in providing validation, commissioning, and quality services, today announced the promotion of Stephanie Welte to Principal Validation Engineer. The Principal Validation Engineer advises clients on best industry practices; defines, plans and executes project work including research, evaluation, and/or solution development to achieve customer objectives; and lead project related functions […]
INDIANAPOLIS, Dec. 7, 2021 /PRNewswire/ — Performance Validation, Inc., a leading national provider of commissioning, qualification, and validation services, today announced that Martin Long has been named as President and Chief Executive Officer effective Jan 1, 2022. Dr. Van Doel, Performance Validations outgoing president will retain his role as Board Chairman, and will retire from Performance Validation in February. Long has more […]
(Indianapolis, IN) Performance Validation, Inc. has acquired 100% of the interests of the Welsh Commissioning Group, Inc. (WCG) headquartered in Auburn, Washington. Structured as a 100 percent employee-owned private company, or an “S corporation employee stock ownership plan” (S ESOP), Performance Validation (PV) credits its success to its employee-owners who operate with a vested interest in […]
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.