Celsis Analytical Services provides cost effective outsourced cGMP laboratory services to industry. We specialize in methods validation and testing for industry, serving companies in biotechnology, pharmaceutical manufacturing, raw materials, and manufacturers of products for consumers, agriculture, veterinary medicine and more. We offer a full range of contract services in analytical chemistry and microbiological testing, plus stability testing and storage programs. And we're up-to-date on ICH and the latest changes to the USP as well as the EP and JP. With U.S.-based facilities in Edison, New Jersey (732) 346-5100 and St. Louis, Missouri (314) 487-6776, Celsis Analytical Services has a uniform commitment to quality and customer service across its operations. Our laboratories are FDA-, USDA-, EPA- and DEA-registered, and function under current Good Manufacturing Practices (cGMP). Celsis Analytical Services laboratories have been successfully audited by both Federal and state regulatory agencies (FDA, EPA, DEA and related state agencies) and 9 of the top 10 worldwide pharmaceutical companies. We encourage your visit, and invite you to contact us to obtain a quote, ask a question or arrange a quality audit at our conveniently located laboratories. Our online sample submission form makes it easier than ever to outsource your routine testing to Celsis.
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