cGMP Consultant provides Registration, U.S. Agent, and Compliance Assistance for U.S. and Non-U.S. Companies manufacturing Food and Beverage, Human or Animal Over the Counter Medicines (OTC), Cosmetics Industries and Medical Devices. cGMP Consultant also assists companies with onsite U.S. FDA Audits and help respond to a 483 or a warning letter. Our consultants come from very vast and vivid backgrounds holding a minimum of Bachelors in Science and 5+ years experience in manufacturing of drugs
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