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From:
10 Mar 2010
To:
10 Mar 2010
Location:
Philadelphia,
USA
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eCTD 2010 |
Compiling new submissions is time consuming and costly to both regulators and drug development organizations. Global regulatory agencies are committed to improving the approval process and the electronic Common Technical Document (eCTD) is seen as a practical solution. At the eCTD2010 conference you can discuss how to prepare your product dossier for global simultaneous eCTD/CTD submissions; You will have a look at tools, tips and taking the mystery out of submission planning and publishing; You will be informed about a case study: Global Submission Management from Concept to Realization; and more.
For more information click here.
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