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cGMP Validation is a full-service validation and compliance firm established in 1997, serving the pharmaceutical, biotechnology, medical device, and animal health industries. The company specializes in the preparation and execution of validation protocols (IQ/OQ/PQ) for equipment, utilities, processes, laboratory instruments, and computer systems. With a team of experienced professionals, cGMP Validation provides integrated compliance solutions, including auditing, risk assessment, and regulatory consulting. Headquartered in Kansas City, the firm has a global reach, having completed over 300 projects across the United States, Canada, and internationally. Their mission is to offer cost-effective, regulatory-sound approaches to validation and compliance to ensure client products meet the highest quality standards. The company has worked with over half of the world's 20 largest pharmaceutical companies, providing tailored services to both small and large manufacturers.
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