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

Philadelphia, PA

CEO Vincent to speak at Facility Design, Innovation and Qualification Conference (Philadelphia, PA)

VTI CEO David W. Vincent, one of the fields leading experts, will be speaking at IVT’s Facility Design, Innovation and Qualification conference, July 29-31, 2014. 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 biopharmaceutical products to the […]

San Diego, CA

ISPE Chapter Event: 14 August 2014 Vendor Night

Come visit our booth at the ISPE Chapter Event: 14 August 2014 Vendor Night. For more information, click here.

San Diego, CA

CEO Vincent to speak at IVT’s Cleaning Validation and Critical Cleaning Processes conference (San Diego, CA)

VTI’s CEO, 20-year veteran David W. Vincent, will share his knowledge and expertise at IVT’s Cleaning Validation and Critical Cleaning Processes conference, being held in Vincent’s home town of San Diego. Cleaning validation has significantly evolved since the late 1980s. Utilizing the knowledge of our elite faculty from four decades of experience, this conference provides […]

Philadelphia, PA

CEO Vincent, speaking at 20th Annual Validation Week, October 28-30, 2014 (Philadelphia, PA)

IVT’s Validation Week celebrates its 20th Anniversary this year! The validation industry’s flagship and best attended event once again provides you the most up-to-date and comprehensive information on new global regulations, technology advances and industry case models for developing, implementing and deploying validation procedures enterprise-wide. VTI CEO, David W. Vincent, will be sharing twenty years […]

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Latest News


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 […]


Design, Construction, Commission, and Qualification Of Critical Utility Systems Part III: HVAC

Environmental control is a critical factor in determining the successful operation of the facility, whether designed for manual or automated operation. Industry experts David Vincent and Herbert Matheson complete their series on critical utility systems, this time focusing on Heating, Ventilation, and Air-Conditioning Systems (HVAC). Download PART III here!  


Design, Construction, Commission, and Qualification Of Critical Utility Systems Part II: Water Systems

“There are various types of water used in the Pharmaceutical Industry. In their multiple uses, such as in actual product formulation, in processing operations, and as a final rinse of product contact surfaces, they can truly be considered product ingredients. Purified water can be produced many different ways and with a range of designs and […]


Design, Construction, Commission, and, Qualification of Critical Utility Systems

“The use of critical utility systems in the pharmaceutical industry is very important to final product quality. That is why the design, construction, commissioning, qualification, and routine monitoring of these systems is important in ensuring that the end product will maintain a reproducible quality. Critical utility systems can be considered the back-bone of any production […]


David W. Vincent, VTI CEO presented at the MD&M the proposed new FDA and USP Regulatory Requirements for the Qualification of Laboratory Instrumentation.