Why VTI?

Validation Technologies, Inc. (VTI), an ISO 9001:2008 Certified Global Company, strives to maintain and inspire professional excellence by providing Validation, Commissioning, and Qualification (C&Q) Services to Pharmaceuticals, Biotechnology, Biologics, Medical Devices and FDA/Internationally regulated industries.  We have the experience, expertise, and commitment to provide the superior service required to meet all of your validation and compliance needs.

We offer a full spectrum of services such as computer validation, cleaning validation, process validation, clean room certification, temperature mapping, process equipment and facility qualification, and much more. Dedication to quality, personalized support and the success of your projects are the foundation of our company.

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Upcoming Events


CEO Vincent to present at IVT’s 6th Annual Validation Week Europe conference in Amsterdam, The Netherlands, March 17-19, 2015

VTI CEO David W. Vincent, one of the fields leading experts, will be speaking at IVT’s 6h Annual Validation Week Europe conference in Amsterdam, The Netherlands, March 17-19, 2015. IVT brings together industry professionals to discuss the latest trends in biopharmaceutical manufacturing facility design. Advances in technology allow for increasingly rapid development and deployment of […]

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Latest News


New Article: Risk Management Analysis Techniques For Validation Programs

In recent years, the subject of quality risk management has become a major focus of the Food and Drug Administration (FDA). On April 9-11 2002, the FDA held a public meeting in Washington, D.C. The purpose of the meeting was for the public to comment on the following three FDA concept papers:  Premarketing Risk Assessment, […]


New article: Quality and Compliance in the Asian Pharmaceutical Industry

VTI CEO David W. Vincent has spent the better part of a decade initiating and directing validation projects in China, a nation quickly becoming prominent in the world pharmaceutical market. His latest article, “Quality and Compliance in the Asian Pharmaceutical Industry,” was just published in the May 2014 issue of the GXP Journal. You don’t […]