Validation Engineering Worldwide
Biotechnology, 1560 Newbury Rd, Thousand Oaks, California, 91320, United States, 1-10 Employees
Who is VALIDATION ENGINEERING WORLDWIDE
Validation Engineering Worldwide Inc (VEWW) provides clients with comprehensive validation testing and compliance packages for use in the Food and Drug Administration (FDA) regulated area...
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Headquarters: 1560 Newbury Rd, Thousand Oaks, California, 91320, United States
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Date Founded: 2003
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Employees: 1-10
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Revenue: Under $1 Million
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Active Tech Stack: See technologies
Industry: Biotechnology
SIC Code: 2834
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Frequently Asked Questions Regarding Validation Engineering Worldwide
Answer: Validation Engineering Worldwide's headquarters are located at 1560 Newbury Rd, Thousand Oaks, California, 91320, United States
Answer: Validation Engineering Worldwide's official website is https://veww.com
Answer: Validation Engineering Worldwide's revenue is Under $1 Million
Answer: Validation Engineering Worldwide's SIC: 2834
Answer: Validation Engineering Worldwide has 1-10 employees
Answer: Validation Engineering Worldwide is in Biotechnology
Answer: Validation Engineering Worldwide contact info: Phone number: Website: https://veww.com
Answer: Validation Engineering Worldwide Inc (VEWW) provides clients with comprehensive validation testing and compliance packages for use in the Food and Drug Administration (FDA) regulated areas of the Pharmaceutical / Biotechnology Industry. The aim of VEWW is to relieve our clients of the burden of producing compliance procedures, regulatory submissions and validation documentation and test execution. VEWW supplies a skilled labor resource to instigate documentation and testing solutions to our clients. We interpret the latest regulations and cGMP to provide our clients with quality documentation and testing packages that provides assurance that all equipment, utilities and automation systems comply with the requirements of cGMP. We also have the specialist resource to carry out audits on Pharmaceutical / Biotechnology facilities to determine the regulatory compliance liabilities and establish solid validation master plans, from which all relevant quality / validation documentation and testing evolves.
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