Preparing for the New Global Requirements for eCTD and Regulated Product Submissions Mastering the Tools and Strategies Paper submissions are losing traction and that's no secret. Every day regulatory authorities across the globe are turning to electronic submissions as their new preferred format ... and the FDA is leading the way. With RPS (Regulated Product Submission) poised to build on the eCTD standard, if you don't yet have your electronic submission process perfected, there's no time to lose. Many drug, biologic and device companies can already measure the difference in dollars — through increased first time acceptance rates, shorter FDA review times, and yes, speed to market.
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