Recently, the Food and Drug Administration (FDA) began accepting electronic filings as standard submissions for the documentation of clinical drug trials. Historically, the FDA and other government agencies have insisted on paper documents, which have presented obstacles for drug makers wanting to automate and streamline their operations. My November 2008 article looks at the automation and technology options that the FDA's new electronic filing policy presents and how life sciences companies are transforming their processes in response.
http://www.managingautomation.com/maonline/magazine/read/view/Ending_the_Endless_Waves_of_Paper_238606
Marty Weil writes for print and the Web. He is a full-time freelancer with more than twenty years of experience writing about the use of technology in numerous fields. He has written extensively about enterprise software and supply chain management. He also covers the interplay between technology and education.
Marty has served as a managing editor for several corporate blog projects. He is also an experienced podcast producer and host.
He is interested in reading, social media, music, and entrepreneurship.
You can contact Marty at marty@martyweil.net.
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12/23/2008
FDA Electronic Filing Article Appears in Managing Automation
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