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Derycz Scientific Featured in Pharmaceutical Manufacturing and Genetic Engineering & Biotechnology News
Date:3/18/2010

published literature for the regulatory approval process can be effectively standardized and facilitated by a dedicated professional document preparation service.  Such a service will not only have specialized expertise in manufacturing information and electronic resources, but will also have a thorough familiarity with both the eCTD format and current copyright laws.

Mr. Derycz commented:  "In these articles I have expressed my belief that dedicated document preparation services play an important role in getting new drugs to market faster.  By smoothing the path to drug approval and minimizing the timeframe involved, pharmaceutical companies and their customers will ultimately reap greater benefits."

To read the Pharmaceutical Manufacturing article online, please visit:

http://www.pharmamanufacturing.com/articles/2010/031.html.

To read the Genetic Engineering &
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