About Us |
About UsAAIPharma Services provides cost-effective, outsourced CGMP-certified laboratory services to industry. We specialize in methods validation and testing for industry, serving biotechnology and pharmaceutical manufacturers, raw materials suppliers 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 Ph EUR and JP. With U.S.-based facilities in Edison, New Jersey (732) 346-5100 and St. Louis, Missouri (314) 487-6776, AAIPharma 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). AAIPharma 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 are pleased to announce that in the FDA's most recent (2009) inspections of our St. Louis (Missouri) and Edison (New Jersey) facilities, not a single Form 483 was issued. Tap into our expertise in CGMP compliance and FDA expectations: we can help. 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 AAIPharma Services. |
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