As a regulatory affairs professional within a research-driven organization, you help keep new product development on track with timely, complete, and accurate data reporting to regulatory authorities – from eCTD submissions for New Drug Applications (NDAs) to Abbreviated New Drug Applications (ANDAs) and beyond.  You also own an important role in the subsequent work to obtain and maintain marketing authorizations for your company’s products, and in ensuring
post-approval compliance on labeling and in advertising.  

Scholarly, peer-reviewed literature is a central component within all of the work you do and supervise – which is where Reprints Desk comes in.  We provide article-focused content workflow service solutions to minimize costly regulatory submission delays and improve compliance visibility:

• eCTD Article Service for the ultra-rapid retrieval and preparation of scientific literature,
  either single articles or batches, for use in Electronic Common Technical Document (eCTD) submissions
• Reprints NRx for enterprise content procurement, inventory management, and reporting related to on-label and off-label article reprints and ePrints usage
• And by early 2010, we’ll have an article repository solution to simplify compliant sharing and re-use of scientific literature

Contact Us Today!
See how we can help you with a complimentary content workflow assessment and to learn why we've been named the top-rated document delivery provider in the 2008 Outsell Document Delivery Best Practices and Vendor Scorecard marketplace survey.