Akorn, Inc. Announces New Center for Excellence
Thursday, October 25, 2007
BUFFALO GROVE, Ill.--(BUSINESS WIRE)--Akorn, Inc. (NASDAQ:AKRX) today announced the signing of a ten-year operating lease for a newly constructed Product Development facility located in Gurnee, IL. This Center for Excellence represents the focal point for centralizing Akorn's New Product Development activities, by consolidating development efforts that are presently managed in Decatur, IL and Somerset, NJ.
Shawn L. Silvestri, Ph.D., Vice President, New Product Development stated, "Our state-of-the art Center for Excellence illustrates the priority and support that New Product Development is given at Akorn. We understand the Research and Development value proposition to the future growth of Akorn, and will now be in a position through this expansion to deliver a pipeline of development projects that complements our current portfolio of branded and generic products.
"This new, state-of-the art facility will position Akorn to compete on a global basis, enabling us to attract and recruit top-tier scientific talent. The facility will conform to the tenets of cGLP (current Good Laboratory Practices) for Research and Development activities and will fulfill all requirements for the development of Akorn's pipeline of NDA and ANDA filings for prescription drug products."
Arthur S. Przybyl, Akorn’s President and Chief Executive Officer stated, "This new Center for Excellence underscores our commitment to new product development activities and to expanding our product pipeline."
About Akorn, Inc.
Akorn, Inc. manufactures and markets sterile specialty pharmaceuticals. Akorn has manufacturing facilities located in Decatur, Illinois and Somerset, New Jersey and markets and distributes an extensive line of hospital and ophthalmic pharmaceuticals. Additional information is available at the Company’s website at www.akorn.com.
Materials in this press release may contain information that includes or is based upon forward-looking statements within the meaning of the Securities Litigation Reform Act of 1995. Forward-looking statements give our expectations or forecasts of future events. You can identify these statements by the fact that they do not relate strictly to historical or current facts. They use words such as "anticipate," "estimate," "expect," "project," "intend," "plan," "believe," and other words and terms of similar meaning in connection with a discussion of future operating or financial performance. In particular, these include statements relating to future steps we may take, prospective products, future performance or results of current and anticipated products, sales efforts, expenses, the outcome of contingencies such as legal proceedings, and financial results.
Any or all of our forward-looking statements here or in other publications may turn out to be wrong. They can be affected by inaccurate assumptions or by known or unknown risks and uncertainties. Many such factors will be important in determining our actual future results. Consequently, no forward-looking statement can be guaranteed. Our actual results may vary materially, and there are not guarantees about the performance of our stock.
Any forward-looking statements represent our expectations or forecasts only as of the date they were made and should not be relied upon as representing our expectations or forecasts as of any subsequent date. We undertake no obligation to correct or update any forward-looking statements, whether as a result of new information, future events or otherwise, even if our expectations or forecasts change. You are advised, however, to consult any further disclosures we make on related subjects in our reports filed with the SEC. In particular, you should read the discussion in the section entitled "Cautionary Statement Regarding Forward-Looking Statements" in our most recent Annual Report on Form 10-K, as it may be updated in subsequent reports filed with the SEC. That discussion covers certain risks, uncertainties and possibly inaccurate assumptions that could cause our actual results to differ materially from expected and historical results. Such factors include, but are not limited to, risks and uncertainties relating to the resolution of the FDA compliance issues at our Decatur, Illinois manufacturing facility. Other factors besides those listed there could also adversely affect our results.
Contact:
Akorn, Inc.
Arthur S. Przybyl
President and CEO
(847) 279-6100
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