Validation Technologies

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Description

VTI has validation experience in Sterile Parenteral Formulation, Biologics (vaccine, blood products), Biotechnology (monoclonal, mammalian, insects, virus, bacterial and plants) and Fill/Finish Facilities for production of small volume injectables as well as experience in cleanroom suites for dispensing, preparation, and filling. We also provide services for the validation of automated CIP/SIP system.

VTI provides an unmatched approach to project management services. The goal of our project management personnel is to produce and implement the most effective programs to meet your unique needs. We’ve done this for numerous companies, and we can do it for you. VTI Project Managers all have significant previous operating company experience with planning, managing and leading various projects and programs.

VTI can help you with all aspects of your cleaning validation program. Our qualified validation consultants have the necessary expertise to develop and improve your cleaning validation methods and procedures. Before beginning our work, we will provide you with clear expectations and deliverables for each step and, of course, customize each process to meet your unique needs.

VTI is committed to continuous improvement of our client services. If your company is a client of VTI, currently or previously, we want to know if our services have met your expectations.

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