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Derycz Scientific Featured In DDN (Drug Discovery News)
Date:1/11/2010

SANTA MONICA, Calif., Jan. 11 /PRNewswire-FirstCall/ -- Derycz Scientific (OTC Bulletin Board: DYSC), a company that is pioneering a fresh way of facilitating the flow of information from content publishers to enterprise customers and their constituents, is featured in an article posted on January 10, 2010, on the website of DDN (Drug Discovery News). The article, written by Derycz Scientific Chairman & CEO Peter Derycz, is titled "Speeding the Path to FDA Approval in the Era of Electronic Submissions." It describes how a dedicated professional document preparation service, such as Derycz subsidiary Reprints Desk, Inc., can help streamline the process for pharmaceutical companies seeking to obtain market approval for a new drug from the U.S. Food and Drug Administration (FDA) and other regulatory agencies around the world.

In the article, Mr. Derycz notes that the FDA now requires all documentation linked with electronic submissions for drug approval to adhere to the electronic Common Technical Document (eCTD) format, an emerging global standard. This requirement poses distinct challenges for a pharmaceutical company because the standard scientific research articles that the company must submit to the FDA as part of the submission process must meet highly specific preparation requirements, and therefore need to be reformatted prior to submission. Reprints Desk, Inc. provides valuable aid in this regard, processing orders for specific research papers and delivering them to a client already formatted to required eCTD specifications.

"The advantages come clear to a pharmaceutical company sharing the eCTD challenge of regulatory submission with a scholarly document service [such as Reprints Desk]," writes Mr. Derycz in the article. "The best step you can take to speed your company's way through the regulatory approval process is to have your regulatory affairs personnel or contract research organizati
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SOURCE Derycz Scientific, Inc.
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